Recalls

Listeria monocytogenes is an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems. Although healthy individuals may suffer only short-term symptoms such as high fever, severe headache, stiffness, nausea, abdominal pain and diarrhea, Listeria infection can cause miscarriages and stillbirths among pregnant women.

The kits were distributed in the following states: AL, AZ, CA, CO, FL, GA, IL, IN, KS, KY, LA, ME, MD, MA, MI, MO, NE, NY, NC, OH, OK, OR, PA, SC, TN, TX, UT, VA, WA, WY.

Reser’s Fine Foods is no longer using any ingredients from the ingredient supplier’s (BrucePac) impacted facility.

Consumers who have purchased these kits should not consume any part of the kits; rather, they may return it to the store for a full refund or discard the item.

Consumers who have questions regarding this recall may call Reser’s Fine Foods at the following number:

Consumer Inquiries:
888-223-2127
Monday-Friday
8:00am – 5:00pm Pacific Time

The recalled Enoki comes in a clear plastic package with the description “Enoki Mushroom” in English and French with the lot code, 4877, on the front in black ink. At the back, there is UPC code 860011505600. The products were distributed from CA and NY through produce distributors or wholesalers to retail stores nationwide.

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

The potential for contamination was noted after routine testing by Maryland State Department of Health revealed the presence of Listeria monocytogenes in 5.3 oz package of Enoki.

The distribution of the product has been suspended.

Consumers who have purchased any package of Enoki with the code 4877 are urged to return them to the place of purchase for a full refund. Consumers with question may contact the company at 718.290.6617, Monday to Friday 8 AM to 4 PM PST.

The ready-to-eat meat and poultry items were produced from June 19, 2024, to October 8, 2024. These products were shipped to other establishments and distributors nationwide then distributed to restaurants and institutions. Details of this recall were updated to include the product list of items with a best by date from 6/19/25-10/8/25.

The products subject to recall bear establishment numbers "51205 or P-51205" inside or under the USDA mark of inspection.

The problem was discovered after FSIS performed routine product testing of finished product containing RTE poultry products produced by BrucePac and confirmed those products positive for Listeria monocytogenes. Subsequent FSIS investigation identified BrucePac RTE chicken as the source of the Listeria monocytogenes.

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

Consumption of food contaminated with L. monocytogenes can cause listeriosis, a serious infection that primarily affects older adults, persons with weakened immune systems, and pregnant women and their newborns. Less commonly, persons outside these risk groups are affected.

Listeriosis can cause fever, muscle aches, headache, stiff neck, confusion, loss of balance and convulsions sometimes preceded by diarrhea or other gastrointestinal symptoms. An invasive infection spreads beyond the gastrointestinal tract. In pregnant women, the infection can cause miscarriages, stillbirths, premature delivery or life-threatening infection of the newborn. In addition, serious and sometimes fatal infections in older adults and persons with weakened immune systems. Listeriosis is treated with antibiotics. Persons in the higher-risk categories who experience flu-like symptoms within two months after eating contaminated food should seek medical care and tell the health care provider about eating the contaminated food.

FSIS is concerned that some product may be available for use in restaurants, institutions, and other establishments. These other establishments may have used affected meat and poultry in RTE products that may be on store shelves or in consumers’ refrigerators or freezers. Restaurants, institutions, and other establishments are urged not to serve or use these products. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify theircustomers 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.

Media and consumers with questions regarding the recall can contact Jeff Golangco, VP Business Development at BrucePac, at 503-874-3000.

Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

Those organisms could lead to serious illness if consumed. Please refer to https://www.fda.gov/food/outbreaks-foodborne-illness/foodborne-pathogens for symptoms descriptions on the pertinent microorganisms.

It is important to note that there have been no reports of illness associated with these products to date. No other production codes or products are affected.

The products affected are indicated below:

The products affected were sold in a 12 fl . oz. RPET plastic bottle shipped in 9ct. corrugated boxes to distributors. The “Enjoy by 12/02/2024” date is located on the bottom part of the bottle, below the label.

This recall has been initiated after complaints of spoiled juices were received.

Consumers who have purchased Happy Moose Juice Tropical Roots 12 fl oz, “Enjoy by: 12/02/2024” or Happy Moose Juice Strawberry Fields 12 fl oz, “Enjoy by: 12/02/2024” are urged to return them to the place of purchase for a full refund.

Consumers with questions may contact the company at 559-797-0252 between 8am and 4:30 pm PST.

The recalled product was distributed to distribution centers in FL, GA, MD and TX and retail locations in: DC, FL, IL, MN, NC, SC, TN, and VA from 8/23/2024 – 09/19/2024.

The product, Gabeez The Big Cheese Snack Mix is packaged in a 3.25-ounce, clear plastic container with a green label, UPC 0 94184 00439 8 and a Best Before date of 04/16/25 stamped on the bottom.

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

The recall was initiated on September 23, 2024 after a customer noticed an incorrect cup. The firm discovered that the tree nut-containing product was distributed in mislabeled packaging that did not reveal the presence of almonds and cashews. The product inside the cup could be Healthy Trails Mix which contains raisins, sunflower seeds, almonds, pumpkin seeds, and cashews.

Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's production and packaging processes.

Customers who have purchased 3.25-ounce packages of the Grabeez The Big Cheese Snack Mix cups with Best Before 041625 are urged to dispose of the product and can submit for a full refund at www.trulygoodfoods.com/grabeezrecall/. Customers with questions may contact the company at marketing@trulygoodfoods.com or 704-602-0610 Monday-Friday 8:00 am – 6:00 pm EST.

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

No illnesses have been reported to date.

The affected 96 oz containers of LACTAID Milk were shipped to retailers and wholesalers from 09/05/24 - 09/18/24 located in AL, CO, CT, FL, GA, IA, IL, IN, KS, KY, LA, MD, MI, MN, MO, MS, NC, NE, NJ, NY, OH, OK, PA, TX, VA, WI, and WY.

The recall applies to a limited number of 96 oz. plastic containers of refrigerated LACTAID Milk with the code 51-4109 P2 and the Best By Date listed in the chart below. The code and Best By Date can be found in the center-top area of the container, as pictured in the image below. This recall applies to only those products that contain the code 51-4109 P2 and the Best By Date specified in the chart below.

Accompanying this release is a photo of the affected product and stamped information on the carton.

This issue was discovered as a result of routine maintenance programs which revealed the potential for trace amounts of almond.

Consumers who purchased the product may return it to the retail location where the purchase was made for a full refund or exchange, or call Hood Consumer Affairs at 800-242-2423 Monday through Friday from 9 AM ET to 5:00 PM ET.

This voluntary recall is being initiated with the knowledge of the US Food and Drug Administration.

Products affected are:

On 8/29/24 the firm was notified by their supplier that the label does not state that the Asafetida used in the product contains wheat.

No illnesses have been reported to date.

The products were distributed on August 20, 2024. These products were packaged in plastic bags and sold in retail stores in Georgia. 

Consumers who have purchased these products are urged not to consume them or they may discard the product. Consumers with questions may contact Biju Joseph at 770-270-1010, Monday - Friday, 11AM- 7PM EST.

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

The beef jerky and bacon jerky products were produced on various dates between Jan. 19, 2024-Aug. 21, 2024. The products were produced without the benefit of inspection by two different owners of the establishment. Ownership changed hands on June 11, 2024. The name of the establishment and the products have remained the same. The products subject to recall are listed here, and the product labels can be viewed here.

The products subject to recall bear establishment number “EST. NO. 34550” inside the USDA mark of inspection. These items were shipped to retail locations in Alabama, Florida, Georgia, North Carolina, Oklahoma, and through internet sales.

The problem was discovered during routine FSIS surveillance activities when it was determined that the establishment continued to produce these jerky products and label them with the USDA mark of inspection after requesting to voluntarily stop FSIS-inspection activities.

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 some product may be in consumers’ pantries. These products should be thrown away or returned to the place of purchase.

FSIS routinely conducts recall effectiveness checks to verify recalling firms notify theircustomers 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 Charles O’Neill, current Co-Owner of Hickory Hollow Jerky at 262-745-5103 or HickoryHollowBeefJerky@gmail.com. Consumers and members of the media can also contact Russ Robbins, previous owner of Hickory Hollow Jerky, at 334-695-5238 or hhjerky@gmail.com.

Consumers with food safety questions can call the toll-free USDA Meat and Poultry Hotline at 888-MPHotline (888-674-6854) or send a question via email to MPHotline@usda.gov. For consumers that need to report a problem with a meat, poultry, or egg product, the online Electronic Consumer Complaint Monitoring System can be accessed 24 hours a day at https://foodcomplaint.fsis.usda.gov/eCCF/.

The recalled snacks were distributed nationwide via retail stores, through online orders at www.bliss-tree.us and through Amazon (www.amazon.com)

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

The recall was initiated after it was discovered that the milk/sesame-containing products was distributed in packaging that did not reveal the presence of milk/sesame. Subsequent investigation indicates the problem was caused by a temporary breakdown in the company's packaging processes.

Production and distribution of the product has been suspended until FDA and the company are certain that the problem has been corrected.

Consumers who have purchased these products are urged to return them to the place of purchase for a full refund.
Consumers with questions may contact the company at 1-732-675-7935 or sales@srilno.com. Available Mon-Fri, 8am - 5pm ET.

The recalled Fudge with nuts branded MONTREAL FUDGE were distributed on 2024-06-19 and 2024-06-20 through MARSHALLS and sold in the retail chains in the below states:

TJ MAXX: Arizona, California, Colorado, New Mexico, Nevada, Utah, Washington, Wyoming.

MARSHALLS: California, Colorado, Connecticut, Delaware, Florida, Georgia, Iowa, Idaho, Illinois, Indiana, Kansas, Kentucky, Louisiana, Massachusetts, Maryland, Michigan, Minnesota, Montana, Mississippi, North Carolina, Nebraska, New Hampshire, New Jersey, Nevada, New York, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin, West Virginia, Wyoming.

The product is packaged in a MONTREAL FUDGE gable box, Chocolate Fudge with nuts 5.6 Oz marked with the lot 0241500805 with expiration date of 2025/MR/01, lot 0241690105 with expiration date of 2025/MR/17, and lot 0241690205 with expiration date of 2025/MR/17, on the back of the box. No other products are impacted by this recall.

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

We initiated this recall after a consumer complained about some mold pieces inside the purchased box and we found also some remaining unpacked sealed products at the manufactured place that had beginning signs of mold.

Consumers who have purchased those affected products are urged to destroy them or to return them to the place of purchase for a full refund. Consumers with questions may contact the company AUTHENTIK FUDGE/MONTREAL FUDGE: info@authentikfudge.com or at phone number (450) 649-1331 / 1 877 313-1331 post 210 or 205.

Monday through Friday, from 8:30 am to 5 pm EST.