Food and Beverage Recalls
Mondelez Global recalls CHIPS AHOY Baked brownie bites
EAST HANOVER, N.J., December 30, 2025 – Mondelēz Global LLC announced today an expansion of its December 24, 2025 voluntary recall in the United States of CHIPS AHOY! Baked Bites Brookie. This expansion includes one additional code date (10MAY2026) and two additional UPCs of product pouches inside the recalled carton units of CHIPS AHOY! Baked Bites Brookie.
This voluntary recall is being conducted because of an incorrect mixing process that resulted in the formation of small corn starch clumps in the product. Due to the characteristics and size of the small starch clumps, the clump could constitute a choking hazard, particularly in special risk groups, such as young children and the elderly.
Prime Food Processing LLC recalls No Brand Dried Croaker Fish
Brooklyn, NY – Prime Food Processing LLC is voluntarily recalling Dried Croaker Fish because the product was not adequately eviscerated, as required by the U.S. Food and Drug Administration (FDA). Fish that are not properly eviscerated may retain internal organs that can harbor harmful bacteria or toxins, posing a potential health risk to consumers.
Reason for Recall: The issue was identified during routine testing conducted by the New York Department of Agriculture. The recall was initiated after the product was selected and sent for regulatory testing. A subsequent investigation determined that the problem originated from an imported product manufactured in Vietnam. At this time, no illnesses or adverse reactions associated with the affected product have been reported.
Medical Device Recalls
Trividia Health, Inc. recalls TRUE METRIX Blood Glucose Monitoring Systems
(FT. LAUDERDALE, FL) – February 6, 2026 – Trividia Health, Inc., announced today that it is initiating a labeling correction which requires a modification of the Owner’s Booklets/System Instructions for Use for all TRUE METRIX, TRUE METRIX AIR, TRUE METRIX GO, and TRUE METRIX PRO Blood Glucose Monitoring Systems (collectively, the “Products”) distributed in the United States, United Kingdom, Mexico, Australia, and the Caribbean.
Trividia is updating the E-5 Error Code in the “Messages” section of the Owner’s Booklets/System Instructions for Use to emphasize that users must seek medical attention immediately if they receive an E-5 error code and are experiencing symptoms of high glucose.
The system displays an E-5 error code for a very high blood glucose event (> 600 mg/dL) or when there is a test strip error. As currently written, the instructions could potentially lead to a delay in treatment if the user does not seek medical attention immediately when they receive an E-5 error code and are experiencing symptoms of high glucose. A delay in treatment may result in serious adverse health consequences or death, especially for users with very high blood glucose levels.
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