#fda-recall
FDA classifies levothyroxine recall over subpotency
The FDA has classified a nationwide levothyroxine recall involving select Major Pharmaceuticals tablets after potency testing found some lots contained less active ingredient than required. The action covers multiple strengths and package sizes used for thyroid treatment. Nationwide levothyroxine recall The U.S. Food and Drug Administration has classified a nationwide recall involving select lo
FDA classifies levothyroxine recall over subpotency
The FDA has classified a nationwide levothyroxine recall involving select Major Pharmaceuticals tablets after potency testing found some lots contained less active ingredient than required. The action covers multiple strengths and package sizes used for thyroid treatment. Nationwide levothyroxine recall The U.S. Food and Drug Administration has classified a nationwide recall involving select lo
Nationwide Cetirizine Recall Covers Four Lots Over Ranitidine Risk
A nationwide cetirizine recall covers four lots of 5 mg allergy tablets distributed by Rising Pharma after red dots and discoloration suggested possible ranitidine contamination. Consumers should check lot numbers, watch for severe allergic reactions and report problems. Unique Pharmaceutical Laboratories has voluntarily recalled four lots of Cetirizine Hydrochloride Tablets USP 5 mg at the consumer level because of potent
Nationwide Cetirizine Recall Covers Four Lots Over Ranitidine Risk
A nationwide cetirizine recall covers four lots of 5 mg allergy tablets distributed by Rising Pharma after red dots and discoloration suggested possible ranitidine contamination. Consumers should check lot numbers, watch for severe allergic reactions and report problems. Unique Pharmaceutical Laboratories has voluntarily recalled four lots of Cetirizine Hydrochloride Tablets USP 5 mg at the consumer level because of potent
Keurig recalls over 80,000 decaf coffee pods that may contain caffeine
Keurig has issued a voluntary recall of more than 80,000 decaf coffee pods after discovering that the products may contain caffeine. The recall applies specifically to K-Cup pods labeled as McCafe Premium Roast Decaf Coffee, with a best-by date of November 17, 2026, and a UPC code of 043000073438. Consumers who purchased these pods are advised to check their inventory, as the product may not meet its labeled decaf specifications. The recall was initially announced on December 6, 2025,
Keurig recalls over 80,000 decaf coffee pods that may contain caffeine
Keurig has issued a voluntary recall of more than 80,000 decaf coffee pods after discovering that the products may contain caffeine. The recall applies specifically to K-Cup pods labeled as McCafe Premium Roast Decaf Coffee, with a best-by date of November 17, 2026, and a UPC code of 043000073438. Consumers who purchased these pods are advised to check their inventory, as the product may not meet its labeled decaf specifications. The recall was initially announced on December 6, 2025,
Multiple tomato brands pulled from shelves across U.S.
The U.S. Food and Drug Administration (FDA) has announced a significant recall of tomatoes across 14 states due to potential salmonella contamination. This recall involves products from two separate companies: Ray & Mascari Inc. and Williams Farms Repack LLC. Ray & Mascari Inc., based in Indiana, has recalled its 4-count Vine Ripe Tomatoes packaged in plastic clamshell containers. These tomatoes were distributed through Gordon Food Service Stores in the following states
Multiple tomato brands pulled from shelves across U.S.
The U.S. Food and Drug Administration (FDA) has announced a significant recall of tomatoes across 14 states due to potential salmonella contamination. This recall involves products from two separate companies: Ray & Mascari Inc. and Williams Farms Repack LLC. Ray & Mascari Inc., based in Indiana, has recalled its 4-count Vine Ripe Tomatoes packaged in plastic clamshell containers. These tomatoes were distributed through Gordon Food Service Stores in the following states
FDA Raises Risk Level for Lay’s Potato Chips Recall Due to Undeclared Milk
In December 2024, the U.S. Food and Drug Administration (FDA) issued an updated warning regarding a voluntary recall of Lay’s Classic Potato Chips due to the presence of undeclared milk. Frito-Lay, the maker of the popular chips, identified a batch of 13 oz bags that may contain milk as an ingredient, which was not disclosed on the packaging. The affected bags, which were sold in Oregon and Washington, carry an expiration date of February 11, 2025. The issue was first raised by a consum
FDA Raises Risk Level for Lay’s Potato Chips Recall Due to Undeclared Milk
In December 2024, the U.S. Food and Drug Administration (FDA) issued an updated warning regarding a voluntary recall of Lay’s Classic Potato Chips due to the presence of undeclared milk. Frito-Lay, the maker of the popular chips, identified a batch of 13 oz bags that may contain milk as an ingredient, which was not disclosed on the packaging. The affected bags, which were sold in Oregon and Washington, carry an expiration date of February 11, 2025. The issue was first raised by a consum









