Recalls

To date there have been no reports of illnesses associated with this recalled product which was distributed nationwide to a limited number of retailers. The company issued the recall out of an abundance of caution after learning of the test results from the FDA.

Per- and polyfluoroalkyl substances (PFAS) are a diverse group of human-made chemicals used in a wide range of consumer and industrial products. PFAS do not easily breakdown and some types have been shown to accumulate in the environment and in our bodies. Available studies suggest associations between PFAS exposure and several health outcomes including but not limited to increased cholesterol levels, increases in high-blood pressure and pre-eclampsia in pregnant women, developmental effects, decreases in immune response, change in liver function, and increases in certain types of cancer.

This recall does not involve any other Bumble Bee products and the company is working with the third-party manufacturer in China to further investigate and resolve this matter. This recall does not affect any other clam products distributed by Bumble Bee.

Consumers who have purchased the recalled products should discard them. Consumers can find the label UPC under the bar code on the back of the package. For any questions regarding the recall or reimbursement, they can contact Bumble Bee Consumer Affairs at 1-888-295-3627 between the hours of 9AM and 6PM EST Monday through Friday, or visit https://www.bumblebee.com/smokedclamrecall/

Following are the product lots impacted by this voluntary recall.

Recalled product was sold as an individual package of 7 ounces. On individual packages, the lot code (best by date) can be found on the back of the bag and the item number (UPC) can be found on the bottom of each package. Photos of the recalled product are below.

This product was distributed nationally at Target. This is the only product that is subject to the recall. Target has been notified and they have removed the product from their store shelves and online.

We were made aware of this issue via a consumer contact. To date, there have been no illnesses reported.

Consumers who purchased the impacted product specified above can contact

Target at 1-800-440-0680, or J&M Foods at 1-800-264-2278 for a refund.

Consumers with questions may contact J&M at 1-800-264-2278.

For media inquiries, reach out to Scott Thibault at sthibault@jm-foods.com

Little Bear brand Vidalia sweet onions (PLU 4159) were available for sale by the pound in:

• Publix stores June 22-24 in Florida and select counties in Georgia,

  Wegmans stores June 23 and 24.in the Rochester, NY area, Massachusetts and two stores in Pennsylvania.

   

   

  See table for more details.

  6lb. bag Vidalia sweet onions , Why FFA Matters brand (Lot#CHW032A and UPC 026303610067. Shipped to Sam’s Club’s retail distribution center in North Carolina. According to Sam’s, all of the recalled onions were destroyed and not available for sale to consumers.

The RTE salami stick with parmesan items were packaged on various dates from October 26, 2021 through April 26, 2022. The following products are subject to recall [view labels]:

2.6-oz. plastic pouches containing “CREMINELLI FINE MEATS salami minis UNCURED ITALIAN SALAMI PARMESAN” with “BEST BY” dates from 06/18/22 through 12/09/22.

The products subject to recall bear establishment number “EST34644” stamped on the back of the product packaging next to the best by date. These items were shipped to retail locations in Arizona, California, Colorado, Florida, Georgia, Illinois, Massachusetts, and Utah, and sold through internet sales nationwide.

The problem was discovered by inspection personnel during a routine label verification review. Egg white lysozyme, a component of the parmesan cheese ingredient, is not declared on the final product label.

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 in consumers’ pantries. 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.

From April 28 to June 17, 2022, approximately 28,000 units of the recalled product were distributed to consumers in the continental United States through online sales and direct delivery, as well as through retail sales at the Daily Harvest store in Chicago, IL and a “pop-up” store in Los Angeles, CA. Samples were also provided to a small number of consumers. Daily Harvest directly notified by email those consumers who were shipped the affected product, and other consumers for whom the company had contact information, and consumers were issued a credit for the recalled product.

Consumers who may still have the recalled product in their freezers should immediately dispose of it.

French Lentil + Leek Crumbles is a frozen product packaged in a 12oz white pouch with the words “Daily Harvest” at the top, a large “CRUMBLES” immediately below the top and the words “French Lentil + Leek” in bold, as shown below. All lot codes of the French Lentil + Leek Crumbles are affected. No other Daily Harvest products are affected or part of this recall.

To date, the company has received approximately 470 reports of illness or adverse reactions. Consumer safety is our highest priority, and we have taken immediate steps to stop production and distribution of the product and conduct a root cause investigation, which is ongoing.

This recall is being made in cooperation with the U.S. Food and Drug Administration.

Consumers who have questions or would like to report adverse reactions should contact Daily Harvest by email at crumbles-recall@daily-harvest.com or by visiting https://www.dailyharvest.com/content/french-lentil-leek-crumbles-advisory# or by calling 1-888-302-0305 9am - 9pm Eastern Time, 7 days a week.

The recalled product was distributed nationwide to 1,049 potential customers through mail orders, and would have been received by customers after June 6, 2022.

The product comes in a 40 gram package marked with lot # D22151011 on the outside of the wrapper.

No illnesses have been reported to date in connection with this recall.

The potential for contamination was noted after routine testing conducted by an accredited third-party laboratory at the request of Built Brands detected the presence of Escherichia coli.

Testing results for additional products made by Built Brands indicate other similar products are not affected and the contamination was an isolated incident, likely resulting from a failure to follow GMP practices.

Consumers who have purchased the product in question are urged to contact the company at questions@built.com for a full refund or replacement. Consumers with questions may also contact the company at questions@built.com or by phone at 1-801- 845-2991 between 8:00 am ' 5:00 pm, Monday-Friday, MST.

The following products are subject to recall, regardless of the product date [View Labels]:

• 13.051 oz. (370g) plastic packages containing “FISH FILLET WITH SPICY SOUP” Freeze Dried Technology Fish. No Preservative.

  12.35 oz. (350g) plastic packages containing “FISH FILLET WITH PICKLED SOUP” Freeze Dried Technology Fish. No Preservative.

   

   

  The products do not bear an establishment number nor a USDA mark of inspection. These items were shipped to retail and wholesale locations nationwide.

  The problem was discovered during a routine FSIS surveillance activity of imported products. China is eligible to import raw Siluriformes products into the United States, but not processed or ready to eat Siluriformes products.

  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.

  FSIS is concerned that consumers may still be in possession of the product. 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.

Salmonella is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Healthy persons infected with Salmonella often experience fever, diarrhea (which may be bloody), nausea, vomiting and abdominal pain. In rare circumstances, infection with Salmonella can result in the organism getting into the bloodstream and producing more severe illnesses such as arterial infections (i.e., infected aneurysms), endocarditis and arthritis.

At the time of this release, there have been no illnesses reported.

This recall affects 50,220 individually wrapped cakes sold in 2 ounce packages and in ten packs of 2 ounce packages of Prairie City Bakery® Peanut Butter Chocolate Chip Ooey Gooey Butter Cake containing cooked peanut butter. They were sold at gas stations and convenience stores nationwide.

The recalled product should not be consumed or handled outside of its package. The product should be disposed of or returned to place of purchase. The recalled product can be identified using the following information:

Product UPC information:

Ten Pack UPC: 7-97884-36719-9

Individual Unit UPC: 7-97884-36718-2

The lot and date codes below are recalled:

The recall was initiated after our copacker who produces and packages this item for Prairie City Bakery was alerted that the peanut butter used had been recalled by Jif.

Consumers who have purchased this product may contact the company at (800) 338-5122 with the package code information for refunds Monday thru Friday, between 9:00 a.m. and 5:00 p.m. Central Time

The recalled "Crabmeat: Jumbo, Lump, Finger, and Claw meat" were distributed to distributors located in Alabama, Georgia, Louisiana, and Mississippi.

The product comes in a 1 lb. containers, package marked with license number AL 111-C with the company name “Irvington Seafood.”

Please look for the following batch number written on the bottom of the container: 130, 131, 132, 134, 137, 139, 141, 144, 145, 146,148, 150

No illnesses have been reported to date in connection with this problem.

The potential for contamination was noted on 05/27/22 after FDA tested on 05/09/22. FDA revealed the presence of Listeria monocytogenes on cooking equipment and cooking room. No crabmeat has been tested but product may have potentially been contaminated with Listeria monocytogenes due to cross contamination. We have decided to do a voluntary recall to ensure the safety of our consumers.

The production of the product has been suspended while FDA and the company continue to investigate the source of the problem.

Consumers who have purchased 1 lb. packages of "Crabmeat" are urged to return them to the place of purchase for a full refund. Consumers with questions may contact the company via email Kammie1101@gmail.com or telephone.