Food and Beverage Recalls
Bazzini, LLC recalls SkinnyDipped Dark Chocolate Coconut Almond Bites
Bazzini, LLC, of Allentown, PA, a co-manufacturer utilized by SkinnyDipped®, is voluntarily recalling a limited number of cases of SkinnyDipped® Dark Chocolate Coconut Almond Bites, out of an abundance of caution, due to the possible presence of undeclared peanut allergen. People who have allergies to peanuts run the risk of a serious or life-threatening allergic reaction if they consume these products.
The recalled products were distributed nationwide and sold through retailers. Some products were also provided as complimentary samples to consumers. The products consist of individually wrapped bites sold in packages of different sizes. Recalled products can be identified by the lot code and Best By (BB) date on the exterior package. Each individually wrapped bite can be identified by the lot code and best by date as shown below:
This recall is limited to only those products identified below. No other SkinnyDipped® products are affected.
Better Weather Activities LLC recalls Better Weather Fix Elixir 15ml
FOR IMMEDIATE RELEASE – May 28, 2026 – Sheridan, Wyoming. Better Weather Actives LLC is voluntarily recalling ALL lots of Better Weather Fix Elixir 15 ml because the products may contain undeclared Mitragynine and Mitragynine Pseudoindoxyl (MP). MP is a more potent derivative of Mitragynine, or Kratom. Consumption of MP can produce undesirable effects such as nausea, vomiting, rapid heart rate (tachycardia), palpitations, hallucinations, sedation, anxiety, and loss of consciousness. It can also fatally suppress the respiratory system. Consumption of Mitragynine, especially MP, may cause addiction with severe opioid withdrawal symptoms. Consumption of products that contain Mitragynine or MP, especially in the context of concomitant use of other drugs (prescribed or illicit), could result in other severe or fatal physiological effects.
The company has not received any reports of adverse events related to this recall to date. The recalled products are packaged in 15 ml bottles packed in display boxes labeled “Better Weather Fix Elixir” and “Better Weather Fix Elixir Berry.”. The recalled products were sold at the consumer level nationwide.
Champion Foods LLC recalls Motor City Pizza Co. 5 Cheese Bread Single and 2 Packs
MAY 29, 2026 – Champion Foods LLC of New Boston, Michigan, is voluntarily recalling certain batches of Motor City Pizza Co. 5 Cheese Bread (“5 Cheese Bread”) because they have the potential to be contaminated with Salmonella. This action follows a California Dairies, Inc. milk powder recall due to a concern of potential Salmonella contamination.
Salmonella is an organism that 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.
De Dios’s Ice Pops II LLC recalls De Dioses Fruit popsicles
PATERSON, N.J. – DE DIOS’S ICE POPS II LLC is voluntarily recalling its 3.7 oz. packages of “popsicles” food treats because they may contain undeclared MILK, YELLOW #5, RED #40, PECANS, AND PISTACHIOS. People who have an allergy or severe sensitivity to these ingredients run the risk of serious or life-threatening allergic reactions if they consume these products.
The recalled products are labeled under the dba: D’DIOSES FRUIT POPS. They were distributed to retail grocery stores in the following states: [N.J., N.Y., P.A., C.T.].
Affected Product Information
This recall applies to all units of the flavors listed below that were produced before the implementation of updated allergen-control procedures (prior to [4/27/2026).
Medical Device Recalls
Dexcom, Inc. recalls Dexcom G7 Continuous Glucose Monitoring System
Dexcom Uncovers Theft of Scrapped Product, Notifies Potentially Impacted Users
- Through ongoing quality and accounting reviews, Dexcom discovered two lots of scrapped product were stolen by a third party before destruction and sold into the market.
- Dexcom is working closely with the FDA and other authorities to ensure patient safety and to investigate the crime.
SAN DIEGO – MAY 26, 2026 – DexCom, Inc. (Nasdaq: DXCM), the global leader in glucose biosensing, announced today through ongoing quality and accounting reviews it recently identified certain lots of Dexcom G7 sensors originally designated as scrap and intended for destruction were stolen during the destruction process, then sold by third parties.
Scrapping limited amounts of sensors that do not meet Dexcom standards is a routine part of the company’s quality control process. Sensors identified as scrap are sent to a third-party vendor for destruction and recycling.
At this time, Dexcom has identified two lots of Dexcom G7 sensors (1725204004 and 1725069002) that were stolen, sold and used by some customers.
Insulet Corporation, Inc. recalls Omnipod Device intended for the subcutaneous delivery of insulin into a patient
ACTON, Mass.--(BUSINESS WIRE)-- Insulet Corporation, Inc. (NASDAQ: PODD) (“Insulet” or the “Company”) today announced a voluntary Medical Device Correction for specific lots of Omnipod® 5, Omnipod DASH®, and Omnipod® Insulin Management System (Omnipod Eros) Pods due to a manufacturing issue, identified through ongoing product monitoring, that could result in insulin under-delivery.
This action is separate from the voluntary Medical Device Correction issued on March 12, 2026 affecting certain Omnipod 5 Pods in the U.S. and includes certain Pod lots distributed in the U.S. and affected international markets.
Pods not included in the affected lots remain safe to use.
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