All articles tagged with #class ii recall
The FDA issued a Class II recall for certain levothyroxine sodium tablets used to treat hypothyroidism after tests found subpotent levels of the active ingredient, potentially reducing effectiveness. Major Pharmaceuticals and Cardinal Health distributed twelve recalled dosages nationwide in cartons; the recall covered multiple lots, but the total quantity was not disclosed.
The FDA is recalling about 244,432 containers of 6.5% carbamide peroxide earwax-removal products distributed nationwide due to subpotent active ingredient, potentially yielding ineffective results. The recall, classified as Class II, covers multiple brands (including CVS Health, Clinere, QC Quality Choice, TopCare Health, Audiologist's Choice, Family Wellness, Good Neighbor Pharmacy, Leader, Foster & Thrive, Meijer, CAREone) and advises consumers not to use these lots until replacement or further guidance is issued.
The FDA issued a recall for three Ventura Foods-produced peanut butter products after detecting blue plastic foreign material, affecting jars sold across 40 states. The recall was reclassified to Class II on Feb 12, 2026. There is no FDA-mandated remedy, but customers can obtain refunds by returning recalled jars to the place of purchase; a full list of affected items is in the recall report.
The FDA has recalled nearly 2,000 cases of 7Up Zero Sugar Tropical Soda due to a labeling error that caused full-sugar soda to be sold as zero sugar, posing health risks especially for diabetics and those managing sugar intake. The recall affects products with specific UPCs and lot numbers, and consumers are advised to check their cans and return any affected products for a refund.