New #foodsafety #recall undeclared #milk #allergen in L & D Market Chicken Wrap Products

L&D Market, Inc. Recalls Chicken Wrap Products Due to Misbranding and Undeclared Allergens

Class I Recall            057-2018
Health Risk: High     Jun 29, 2018

Congressional and Public Affairs
Sarah R. Lichtman
(202) 720-9113
Press@fsis.usda.gov

The wasabi chicken wrap items were produced on June 21, June 26 and June 27, 2018. The following products are subject to recall: [View Labels (PDF only)]

  • 7.5-oz. plastic wrapped packages containing “Fresh. LOCAL. TASTY. EVERY DAY. WASABI CHICKEN WRAP,” with “SELL BY” dates of June 25, June 30 and July 1, 2018.
  • 7.5-oz. plastic wrapped packages containing “In-House Marketplace WASABI CHICKEN WRAP,” with a “SELL BY” date of June 25, 2018.

The products subject to recall bear establishment number “P-40171” inside the USDA mark of inspection. These items were shipped to retail locations in Cambridge, Massachusetts.

The problem was discovered by FSIS personnel during routine in-plant verification activities.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

FSIS is concerned that some product may be in consumers’ refrigerators. Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify that recalling firms are notifying their customers of the recall and that actions are being taken to make certain that the product is no longer available to consumers. When available, the retail distribution lists will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Consumers and members of the media with questions about the recall can contact Freddy Noviello, Plant Manager, L&D Market, Inc., at (617) 567-9725.

New #foodsafety #recall undeclared #egg & #milk #allergen in Wish-Bone House Italian Salad Dressing

Wish Bone Salad Dressing Issues Allergy Alert On Undeclared Milk and Egg in 15 oz. Wish-Bone House Italian Salad Dressing

For Immediate Release

June 28, 2018

Contact

Consumers

Pinnacle Foods Consumer Care
1-888-299-7646

Media

Janice Monahan
Mediainquiries@pinnaclefoods.com
973-541-8620
973-718-7068 x1

Announcement

Pinnacle Foods Inc. is voluntarily recalling a limited quantity of Wish Bone House Italian Salad Dressing 15 oz. with the health and safety of our consumers as our top priority. The recall was initiated after learning from a retail customer that a limited number of bottles were mislabeled. The product contains milk and egg, known allergens not declared on the bottle. People who have an allergy or severe sensitivity to milk or egg may run the risk of a serious or life-threatening allergic reaction if they consume this product. If you are not allergic to milk or egg, this product is safe to eat. No illnesses have been reported to date. The Food and Drug Administration has been made aware of this recall.

No illnesses have been reported to date, but the company is taking this action as part of its commitment to the health and safety of its customer.

The product was produced on March 19, 2018. In total, 7,768 cases of Wish-Bone House Italian Salad Dressing in 15 oz. bottles, distributed nationwide, are involved in the recall. The “Best If Used By” date can be found on the neck label of the bottle. No other Wish-Bone products are included in this recall. Specific details of the product being recalled are outlined below.

All affected distributors and retail customers, as well as the Food Allergy & Anaphylaxis Network (FAAN), are being notified and the affected product is being removed from store shelves.

The recalled items can be identified by a “Best If Used By” date printed on the neck wrapper. Only products with a “Best If Used By” date of Jan 13 19 and with labeling that matches both the front and back labels attached in the press release are subject to recall.

FLAVOR CASE LOT
CODE
ITEM NUMBER # Best if Used By Date
(found on neck label of bottle)
Wish Bone House Italian 6/15 oz. 4913019S51 004132100648 Jan 13 19

There is no impact on any other Italian varieties and no other products produced by Pinnacle Foods are affected by this recall.

Consumers should not consume these products. Affected product may be returned to the place of purchase for a full refund. Consumers with questions may contact Pinnacle Foods at 1-888-299-7646. Hours: Daily between 9 a.m. and 5 p.m. Eastern Time.

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New #foodsafety #recall of Sparkling Ice® Cherry Limeade due to Customer Complaints

Talking Rain® Voluntarily Recalls Sparkling Ice® Cherry Limeade in Response to Customer Complaints

For Immediate Release

June 28, 2018

Contact

Consumers

1-855-201-4333

Media

Greg Menken
1 616-878-2830

Announcement

Talking Rain® (the Company) is voluntarily recalling specific lot codes of bottles of its Sparkling Ice® Cherry Limeade beverage in response to a small number of customer complaints that reported an off-taste and off-odor of the affected product. The Company made the decision to recall the product out of an abundance of caution. No other Sparkling Ice products are affected by this recall.

The Sparkling Ice Cherry Limeade product subject to recall was produced only at one of the Company’s facilities that make this product. The product comes in a 17 ounce clear plastic bottle under the name Sparkling Ice Cherry Limeade. The product is sold as a single item, as well as in multipacks of the affected product and in multipacks containing a variety of other unaffected flavors. The product subject to recall can be identified by the following information that is displayed on the neck of the bottle. All other products made by the Company are not part of this voluntary recall.

Affected product labeling:

Bottle Lot Code Expiration Date on Bottle Expiration Date Bottle UPC Case/Variety Pack UPCs
8064-63 120518 12/5/18 01657195084 016571950866
8065-63 120618 12/6/18 016571950927
8079-63 122018 12/20/18 016571951283
8080-63 122118 12/21/18 016571950866
8087-63 122818 12/28/18 016571953126
8088-63 122918 12/29/18 016571953614
8089-63 123018 12/30/18
8112-63 012219 01/22/19
8113-63 012319 01/23/19
8114-63 012419 01/24/19
8118-63 012819 01/28/19
8119-63 012919 01/29/19
8126-63 020619 02/06/19
8131-63 021119 02/11/19
8132-63 021219 02/12/19
8144-63 022419 02/24/19
8145-63 022519 02/25/19
8146-63 022619 02/26/19
8165-63 031419 03/14/19
8166-63 031519 03/15/19
8167-63 031619 03/16/19

Talking Rain learned of the issue after a small number of customers brought their concerns to the company’s attention. Talking Rain is currently investigating the cause of the issue in collaboration with the U.S. Food and Drug Administration (FDA).

Consumers who purchased the affected product are advised not to drink it and to call the Talking Rain customer center at 855-201-4333 to receive a coupon to replace their purchase.

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Updated #foodsafety #investigation of Romain Lettuce E.coli O157:H7 outbreak & infections

FDA Investigating Multistate Outbreak of E. coli O157:H7 Infections Linked to Romaine Lettuce from Yuma Growing Region

June 28, 2018

The U.S. Food and Drug Administration, along with the Centers for Disease Control and Prevention (CDC) and state and local partners, are investigating a multistate outbreak of E. coli O157:H7 illnesses linked to romaine lettuce from the Yuma growing region.

Update

The FDA, along with CDC and state partners, initiated an environmental assessment in the Yuma growing region to further investigate potential sources of contamination linked to this outbreak.

Samples have been collected from environmental sources in the region, including water, soil, and cow manure. Evaluation of these samples is ongoing.

To date, CDC analysis of samples taken from canal water in the region has identified the presence of E. coli0157:H7 with the same genetic finger print as the outbreak strain. We have identified additional strains of Shiga-toxin producing E. coli in water and soil samples, but at this time, the samples from the canal water are the only matches to the outbreak strain.

Analysis of additional samples is still ongoing, and any new matches to the outbreak strain will be communicated publicly and with industry in the region.

Identification of the outbreak strain in the environment should prove valuable in our analysis of potential routes of contamination, and we are continuing our investigation in an effort to learn more about how the outbreak strain could have entered the water and ways that this water could have come into contact with and contaminated romaine lettuce in the region.

Fast Facts

  • The FDA is investigating a multistate outbreak of E. coli O157:H7 illnesses linked to romaine lettuce sourced from the winter growing areas in and around the Yuma growing region. Suspect product is no longer being harvested or distributed from this area and is no longer available in stores or restaurants, due to its 21-day shelf life.
  • As of June 27, the CDC reports that 210 people in 36 states have become ill. These people reported becoming ill in the time period of March 13, 2018 to June 6, 2018. There have been 96 hospitalizations and five deaths.
  • The traceback investigation indicates that the illnesses associated with this outbreak cannot be explained by a single grower, harvester, processor, or distributor. While traceback continues, the FDA will focus on trying to identify factors that contributed to contamination of romaine across multiple supply chains.  The agency is examining all possibilities, including that contamination may have occurred at any point along the growing, harvesting, packaging, and distribution chain before reaching consumers.
  • On May 31, 2018 the FDA released a blog with updated information on the traceback investigation (for additional information, visit FDA Update on Traceback Related to the E. coli O157:H7 Outbreak Linked to Romaine Lettuce).
  • The FDA, along with CDC and state partners, initiated an environmental assessment in the Yuma growing region to further investigate potential sources of contamination linked to this outbreak. To date, CDC analysis of samples taken from canal water in the region has identified the presence of E. coli 0157:H7 with the same genetic finger print as the outbreak strain. We have identified additional strains of E. coli in water and soil samples, but at this time, the samples from the canal water are the only matches to the outbreak strain.
  • The FDA is continuing to investigate this outbreak and will share more information as it becomes available.
  • Consumers who have symptoms of STEC infection should contact their health care provider to report their symptoms and receive care. Although many infections resolve in 5-7 days, they can result in serious illness, including a potentially serious condition called hemolytic uremic syndrome.
  • The current outbreak is not related to a recent multistate outbreak of E. coli O157:H7 infections from November to December 2017 linked to leafy greens consumption. People in the previous outbreak were infected with a different DNA fingerprint of E. coli O157:H7 bacteria.

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What is the Problem and What is being Done About It?

The FDA and the CDC, along with state and local health officials, are investigating an outbreak of Shiga toxin-producing E. coli O157:H7 infections.

There are 210 cases in 36 states: Alabama (3) Alaska (8), Arkansas (1), Arizona (9), California (49), Colorado (3), Connecticut (2), Florida (3), Georgia (5), Idaho (12), Illinois (2), Iowa (1), Kentucky (1), Louisiana (1), Massachusetts (4), Michigan (5), Minnesota (12), Mississippi (1), Missouri (1), Montana (9), Nebraska (1), New Jersey (8), New York (11), North Carolina (1), North Dakota (3), Ohio (7), Oklahoma (1), Oregon (1), Pennsylvania (24), South Dakota (1), Tennessee (3), Texas (4), Utah (1), Virginia (1), Washington (8), and Wisconsin (3). The current outbreak is not related to a recent multistate outbreak of E. coli O157:H7 infections linked to leafy greens. People in the previous outbreak were infected with a different DNA fingerprint of E. coli O157:H7 bacteria.

The most recent information collected by the FDA, in conjunction with federal, state, and local partners, indicates that the romaine lettuce that ill people ate was likely grown or originated from the winter growing areas in or around the Yuma region. This region generally supplies romaine lettuce to the U.S. during November-March each year.

The FDA is working closely with federal, state, and local partners on an ongoing traceback investigation to determine the source of romaine lettuce supplied to ill consumers.  In a typical traceback effort, CDC and the FDA identify clusters of people who became ill, especially in different geographical regions and work to trace the food eaten by those made ill to a common source. For this outbreak investigation, we have been able to identify romaine lettuce as the common food source.  Romaine products that would have caused illness were no longer available at exposure locations, making it difficult to determine production lots of concern.  In addition, we have found that a single production lot may contain romaine from multiple ranches, which makes the traceback more challenging. We are working with federal and state partners and companies as quickly as possible to collect, review and analyze hundreds of records in an attempt to traceback the source of the contaminated romaine lettuce.

To date, the available information indicates that romaine lettuce from the Yuma growing region is the source of the current outbreak of E. coli O157:H7 infections, and was supplied to restaurants and retailers through multiple processors, grower/shipper companies, and farms. The information we have collected indicates that the illnesses associated with this outbreak cannot be explained by a single grower, harvester, processor, or distributor.  While traceback continues, FDA will focus on trying to identify factors that contributed to contamination of romaine across multiple supply chains.  The agency is examining all possibilities, including that contamination may have occurred at any point along the growing, harvesting, packaging, and distribution chain before reaching consumers. (for additional information, visit FDA Update on Traceback Related to the E. coli O157:H7 Outbreak Linked to Romaine Lettuce).

The traceback investigation is ongoing and additional information will be provided as it becomes available.

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Timeline

On April 4, 2018 FDA learned about a cluster of E. coli O157:H7 infections in two states.

On April 5, 2018 a new cluster was reported in multiple states.

In the following weeks, the FDA, CDC, and state partners worked together to collect additional information and conduct traceback activities to identify a food item of interest.

On April 10, 2018 the FDA publicly communicated about the outbreak, but was unable to identify a food source. The agency recommended that consumers practice safe food handling and preparation and to consult a health care provider if they think they might have symptoms of E. coli infection.

Interviews with ill people allowed health partners to identify chopped romaine from the Yuma growing region as the likely source of contamination on April 13, 2018.

*April 16, 2018 was the final day of romaine harvesting in the Yuma growing region, however at the time chopped romaine had just been identified as the likely source allowing the traceback investigation to begin and at this point, nospecific farms in the Yuma region had been identified. FDA did not receive confirmation of the final harvest date until May 2, 2018.

On April 19, 2018, Alaska health partners announced that eight persons with E. coli O157:H7 infections from a correctional facility have been confirmed as part of the outbreak. These individuals ate whole-head romaine lettuce from the Yuma growing region. Following this announcement the FDA advised consumers to avoid all romaine lettuce from the Yuma growing region.

In the following weeks FDA continued its traceback investigation, part of which was able to trace the Alaskan correctional facility back to a single farm, which was released on April 27, 2018.

On May 2, 2018 the FDA received confirmation from the Arizona Leafy Greens Marketing Agreement that romaine lettuce was no longer being produced and distributed from the Yuma growing region, reducing the potential for exposure to contaminated product. At that time, due to the 21-day shelf life, we could not be certain that romaine lettuce from that region was no longer in the supply chain.

On May 31, 2018 the FDA released a blog with updated information on our ongoing traceback investigation (for additional information, visit FDA Update on Traceback Related to the E. coli O157:H7 Outbreak Linked to Romaine Lettuce).

From June 4 – June 8, 2018 sampling for the environmental assessment was conducted in the Yuma growing region.

On June 28, 2018 the CDC announced that the outbreak has ended. In addition, the FDA and CDC announced preliminary sample results from the environmental assessment of the Yuma growing region.

What are the Symptoms of E. coli O157:H7 Infection?

The symptoms of STEC infections vary for each person but often include severe stomach cramps and bloody diarrhea. If there is fever, it is usually not very high (less than 101 degrees Fahrenheitdisclaimer icon /less than 38.5 degrees Celsius). Most people get better within 5–7 days. Some infections are very mild, but others are severe or even life-threatening.

Around 5–10 percent of those who are diagnosed with STEC infection develop a potentially life-threatening complication, known as hemolytic uremic syndrome (HUS).

Symptoms of HUS include fever, abdominal pain, feeling very tired, decreased frequency of urination, small unexplained bruises or bleeding, and pallor. Most people with HUS recover within a few weeks, but some suffer permanent damage or die. People who experience these symptoms should seek emergency medical care immediately. Persons with HUS should be hospitalized because their kidneys may stop working (acute renal failure), but they may also develop other serious problems such as hypertension, chronic kidney disease, and neurologic problems.

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Who is at Risk?

People of any age can become infected with Shiga toxin-producing (STEC) E. coli. Children under the age of 5 years, adults older than 65, and people with weakened immune systems are more likely than others to develop severe illness, including HUS, but even healthy older children and young adults can become seriously ill.

What Do Restaurants and Retailers Need To Do?

Retailers, restaurants, and other food service operators should always take steps to avoid the cross contamination of cutting surfaces and utensils through contact with potentially contaminated products. Retailers, restaurants, and other food service operators should always take steps to adequately control the temperature of cut leafy greens and to avoid cross contamination of cutting surfaces and utensils through contact with potentially contaminated products. To prevent cross contamination, you should follow the steps below:

  • Wash and sanitize display cases and refrigerators where potentially contaminated products were stored.
  • Wash and sanitize cutting boards, surfaces, and utensils used to prepare, serve, or store potentially contaminated products.
  • Wash hands with hot water and soap following the cleaning and sanitation process.
  • In accordance with the FDA Food Code 2017, cut leafy greens, including romaine lettuce,  require time/temperature control for safety and should be refrigerated at 41°F or lower.

Regular frequent cleaning and sanitizing of food contact surfaces and utensils used in food preparation may help to minimize the likelihood of cross-contamination.

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What Do Consumers Need To Do?

Consumers should always practice safe food handling and preparation measures. It is recommended that they wash hands, utensils, and surfaces with hot, soapy water before and after handling food.

For refrigerators and other food preparation surfaces and food cutting utensils that may have come in contact with contaminated foods, it is very important that the consumers thoroughly clean these areas and items.

Consumers should follow these simple steps:

  • Wash the inside walls and shelves of the refrigerator, cutting boards and countertops; then sanitize them with a solution of one tablespoon of chlorine bleach to one gallon of hot water; dry with a clean cloth or paper towel that has not been previously used.
  • Wash hands with warm water and soap for at least 20 seconds before and after handling food.
  • Wipe up spills in the refrigerator immediately and clean the refrigerator regularly.
  • Always wash hands with hot, soapy water following the cleaning and sanitization process.
  • Persons who think they might have become ill from eating potentially contaminated foods should consult their health care provider.

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Who Should be Contacted?

People who think they might have symptoms of an E. coli infection should consult their health care provider.

People with questions about food safety can call the FDA at 1-888-SAFEFOOD or consult the fda.gov website: http://www.fda.gov.


Additional Information

New #foodsafety #recall undeclared #almond #allergen in Oregon Peppermint Cacao Nectar Bar

Nectar Foods Inc Dba Honey Mama’s Issues Allergy Alert on Undeclared Almonds in Oregon Peppermint Cacao Nectar Bar

For Immediate Release

June 22, 2018

Contact

Consumers

Nectar Foods Inc.
1-888-506-2627

Media

Mollie Harger
503-799-1780

Announcement

Nectar Foods Inc., DBA Honey Mama’s of Portland, Oregon is recalling 79 Sleeves (948 units) of Oregon Peppermint bars, lot code 112918, because it may contain undeclared almonds.  People who have an allergy or severe sensitivity to almonds run the risk of serious or life-threatening allergic reaction if they consume this product.

Oregon Peppermint Bars were distributed in Arkansas, California, Delaware, Florida, Georgia, Louisiana, Massachusetts, New Jersey, New York, North Carolina, Ohio, Oregon, Texas, Utah, Virginia, Vermont, Washington and Wisconsin through retail stores and website sales through HoneyMamas.com between June 1st, 2018 and June 21st, 2018.

The product can be identified by name and label listing flavor as Oregon Peppermint. The label is blue with white script and a dark blue Honey Mama’s hummingbird logo. Bars are wrapped in brown freezer paper and sealed with label, measuring 3×3 inches, and approximately 8mms thick. Product UPC is 8 54835 00402 9. Bars are refrigerated or frozen, with expiration code 112918 is printed on white label on reverse of bar.

No illnesses have been reported to date related to this recall.

The recall was initiated after it was discovered that product containing almonds was distributed in packaging that did not reveal the presence of almonds.

This recall is being made with the knowledge of the U.S. Food and Drug Administration.

Consumers who have purchased the affected Honey Mama’s Oregon Peppermint bars, and have an allergy or severe sensitivity to almonds, are urged to return it to the place of purchase for a full refund or destroy product.

Consumers with questions may contact the company at 1-888-506-2627 from 9am to 5pm PST, Monday-Friday. After hours/weekend calls can leave a voicemail and messages will be responded to in the order they were received.

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New #foodsafety #recall of 10,805 lbs of canned chicken gravy products possible underprocessing

Aunt Kitty’s Foods Inc. Recalls Canned Chicken Products Due to Possible Processing Deviation

Class I Recall056-2018
Health Risk: HighJun 26, 2018

Congressional and Public Affairs
Benjamin A. Bell
(202) 720-9113
Press@fsis.usda.gov

WASHINGTON, June 26, 2018 – Aunt Kitty’s Foods, Inc., a Vineland, N.J. establishment, is recalling approximately 10,805 pounds of canned chicken gravy products due to a possible processing deviation that may have led to underprocessing of products, the U.S. Department of Agriculture’s Food Safety and Inspection Service (FSIS) announced today.

The canned chicken gravy was produced on April 4, 2018. The following products are subject to recall: [View Labels(PDF only)]

  • 10.5-oz. canned “Western Beef Chicken GRAVY” with lot codes 1809515, 1809525, 1809535, and 1809545 and a best by date of June 2021.
  • 10.5-oz. canned “ShopRite Chicken GRAVY” with lot code 1809515, 1809525, 1809535, and 1809545 and a best by date of June 2021.
  • 10.5-oz. canned “Price Rite Chicken GRAVY” with lot code 1809515, 1809525, 1809535, and 1809545 and a best by date of June 2021.

The products subject to recall bear establishment number “P-864” inside the USDA mark of inspection. These items were shipped to retail locations in New Jersey and New York.

The problem was discovered on June 19, 2018 during the establishment’s labeling process, which detected multiple bulging cans of chicken gravy. FSIS was notified on June 21, 2018.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution lists will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Consumers and members of the media with questions about the recall can contact Craig Adams, Vice President of Quality Assurance, Aunt Kitty’s Foods, Inc. (717) 634-3198.

New #foodsafety #recall of 13,554 lbs of elk, bison and beef meat stick products produced without approved voluntary grant of inspection

People’s Sausage Co. Recalls Jerky and Meat Stick Products Produced without an Approved Voluntary Grant of Inspection

Class I Recall055-2018
Health Risk: HighJun 25, 2018
Congressional and Public Affairs

Benjamin A. Bell
(202) 720-9113
Press@fsis.usda.gov

The shelf stable elk and bison jerky and meat stick products were produced on various dates from May 3, 2016 through June 15, 2018. The following products are subject to recall: [View Labels (PDF only)]

  • 4-oz plastic bags containing “MONTRAIL BISON WILD STICKS Hot and Spicy” with a use by date from May 3, 2018 to June 15, 2020.
  • 3-oz plastic bags containing “MONTRAIL BISON LLC. Elk Jerky Lemon Chile” with a use by date from May 3, 2018 to June 15, 2020.
  • 3-oz plastic bags containing “MONTRAIL BISON LLC. Elk Jerky Teriyaki” with a use by date from May 3, 2018 to June 15, 2020.
  • 3-oz plastic bags containing “MONTRAIL BISON Elk Jerky Sweet and Spicy” with a use by date from May 3, 2018 to June 15, 2020.
  • 3-oz plastic bags containing “MONTRAIL BISON Elk Jerky Old Fashioned” with a use by date from May 3, 2018 to June 15, 2020.
  • 3-oz plastic bags containing “MONTRAIL BISON LLC. Bison Jerky Lemon Chile” with a use by date from May 3, 2018 to June 15, 2020.
  • 3-oz plastic bags containing “MONTRAIL BISON LLC. Bison Jerky Teriyaki” with a use by date from May 3, 2018 to June 15, 2020.
  • 3-oz plastic bags containing “MONTRAIL BISON LLC. Bison Jerky Sweet and Spicy” with a use by date from May 3, 2018 to June 15, 2020.
  • 3-oz plastic bags containing “MONTRAIL BISON LLC. Bison Jerky Old Fashioned” with a use by date from May 3, 2018 to June 15, 2020.

The products subject to recall bear establishment number “EST. 4160” inside the triangle shaped USDA mark of inspection. These items were shipped to retail locations in Montana.

The problem was discovered on June 22, 2018 during an FSIS investigation.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.

Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Consumers and members of the media with questions about the recall can contact Mark Bianchetti, President, People’s Sausage Co., at (213) 627-8633.

Dining Review: Trail Crest Brewery

The first time I went to Trail Crest Brewery, was November 22nd, 2017. I didn’t do a full review, but I did post the following on Facebook that evening: Heard some sketchy reviews, decided to check it out. New menu, change in items, got rid of chef. Looks like they have made some good changes. My food was really good.

Since that time, I had not returned, even though the Trail Crest social media had been messaging about how good their burgers were every time I would post about having a burger. Recently, Trail Crest Brewery started a Monday event called “Mug Shot Monday”. Get a mug of beer and a flavored infused shot for $7.50 and they will take your picture and place it on their wall. I will be the first to admit that I am not much of an alcohol person, and I really don’t care that much for beer, either. But, since it is a fun promotion, I decided to go and give it a try and see if the food had changed any since my last visit. I ordered the Trail Crest Rickety Trail and a shot of butterscotch Schnapps (whiskey was not included in special, sorry brother & sister Boilermakers).

For my meal, some of you know I can be extremely outlandish (although some people have called me an a$$hole). In reality, I am a person that generally knows what I want and will ask for it. Having worked in the food service industry for over 30 years, I know that some things are possible and I know that some things are not. You never know unless you ask.

The menu at Trail Crest has lots of interesting items, most of which I don’t understand being on a menu at a brewery, but it the owner that decided on these items, and it may actually work for them. I looked through the burger section, as I was there for a burger, and found that they have a chili burger. Now, I will admit that I LOVE chili, especially on a burger, but as I said, I can be a bit outlandish, so I started asking if I could have them make it a special way for me. I can hear some of my friends rolling their eyes and saying “oh, he’s going to try and make his monstrosity chili burger.” and they would be absolutely correct.

The Doctor Mc Keown Monstrosity Burger is built from the bottom up, starting with the bun and a hamburger patty cooked and placed on each bun slice. Each burger gets a slice of cheese, for this one, I went with pepper-jack. A fried egg is then placed on top of the cheese. I generally ask for the eggs to be cooked over-medium (firm white, runny yoke); however, we did not discuss the egg and one came out over-medium the other came out over-hard (both white and yoke firm). On top of the egg I generally place jalapenos, but they only had hatch green chilies, so I went with that. Next, the entire entree is covered in Texas style chili, then topped with cheddar cheese. Trail Crest also adds sour cream and green onions on top, which added a nice touch. The meal at Trail Crest was served with shoestring french fries.

I was very happy that they were able to do a good recreation of the Dr. Mc Keown Monstrosity Burger. The bun was a beer bread. The green hatch chilies added some spice to the entree; however, there was very little flavor anywhere else. I scrapped everything off the burger and tried tasting just the burger and it had almost no flavor that I could ascertain. I am not sure if they put any seasoning in or on the burger when it is cooking, because I couldn’t taste anything. The burger was cooked to a nice medium-rare, which generally leaves the flavor of the meat, but there was nothing. The chili had some flavor to it, however, it was not as pronounced as I would have expected a Texas style chili to be. Having been a chili judge for several competitions around the country, I probably expected more flavor (or even spice), and I understand that a lot of people can’t handle spicy chili or even chili with too much flavor.

Overall, I would say that the burger wasn’t too bad. I did finish all of it (except the bread) and some of the fries. I enjoyed my visit to the location and my server, Jessica, was knowledgeable, patient, and very nice to work with.

New #foodsafety #recall of 4,944 lbs of Black Forest Ham products labeled as Honey Smoked Turkey Breast

Recall Notification Report 054-2018 (Pork Products)

Class III Recall054-2018
Jun 25, 2018
Congressional and Public Affairs

Benjamin A. Bell
(202) 720-9113
Press@fsis.usda.gov

The Premium Black Forest Ham products were produced on April 27, 2018. The following products are subject to recall: [View Label (PDF only)]

  • 1-lb. plastic gas-flushed resealable packages containing a single ham labeled “Land O’Frost PREMIUM Old World Style Black Forest Ham” with Lot 8117D and a sell-by date of August 10, 2018 on the label.

The products subject to recall bear establishment number “Est.500K” inside the USDA mark of inspection. These items were shipped to a retail locations in Arizona, California, Oregon, Texas, and Washington.

The problem was discovered on June 20, 2018 after the firm received a consumer complaint about the product. The firm notified FSIS of the problem on June 22, 2018.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about an injury or illness should contact a healthcare provider.

FSIS routinely conducts recall effectiveness checks to verify that recalling firms are notifying their customers of the recall and that actions are being taken to make certain that the product is no longer available to consumers.

Consumers and members of the media with questions about the recall can contact Dar Gautreaux, Administrative Assistant with Land O’Frost, at (800) 762-9865.

New #foodsafety #recall of 258,121 lbs of pork lard products produced without inspection

Quay Corporation Recalls Pork Products Produced Without Benefit Of Inspection

Class I Recall053-2018
Health Risk: HighJun 22, 2018
Congressional and Public Affairs

Benjamin A. Bell
(202) 720-9113
Press@fsis.usda.gov

The shelf stable packaged pork lard products were produced on July 29, 2016 through June 22, 2018. The following products are subject to recall:  [View Labels (PDF only)]

• 28-oz. sealed plastic cups containing “MARGARITA MANTECA PORK LARD” with sell by dates ranging from Jan. 29, 2017 through Dec. 22, 2018.

The products subject to recall bear establishment number “EST. 17445” inside the USDA mark of inspection. These items were shipped to retail locations in Texas.

The problem was discovered when FSIS personnel visited the establishment after receiving information that the product was being labeled for sale without inspection.

There have been no confirmed reports of adverse reactions due to consumption of these products. Anyone concerned about a reaction should contact a healthcare provider.

Consumers who have purchased these products are urged not to consume them. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify their customers of the recall and that steps are taken to make certain that the product is no longer available to consumers. When available, the retail distribution list(s) will be posted on the FSIS website at www.fsis.usda.gov/recalls.

Consumers and members of the media with questions about the recall can contact Victor Cuellar, Operations Manager, Quay Corporation, at (847) 676-4233.