Severity 2 of 5
Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.
Severity 2 (Moderate) recalls cover minor labeling errors, low-risk contamination, and voluntary precautionary recalls. The agency's own classification is typically FDA Class III, or the issue is something like incomplete instructions or a small UPC mismatch where the product itself is safe but doesn't meet documentation requirements. Use the same brand-name product safely; follow the manufacturer's instructions for return or exchange if you want a refund.
The full rubric is on the methodology page. Severity is computed deterministically from the agency’s own classification plus the source text — no editorial vibes.
GM Manufacturing is recalling Albert Capsules dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
GM Manufacturing is recalling 502 units of Una De Gato dietary supplements found in California due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
GM Manufacturing is recalling Garcinia Series Capsules due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
GM Manufacturing is recalling 5,000 units of Platinum B dietary supplements in California due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
GM Manufacturing is recalling Nano Papa dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
GM Manufacturing is recalling Tendon & Muscle Plus dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
GM Manufacturing is recalling 829 units of Garcinia Cambogia dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
GM Manufacturing is recalling Maxium and Prolong capsules due to significant violations of dietary supplement manufacturing regulations.
Teleflex Medical is recalling 120 units of Emerald Fiberoptic Blades because the boxes contained incorrect Miller 4 blades instead of the labeled Macintosh 4 blades.
GM Manufacturing is recalling Detoxification Plus dietary supplements due to significant violations of current good manufacturing practice (cGMP) regulations.
Dermamedics, L.L.C. is recalling specific Complexion Repair Topical Rehydrating Emulsions because the FDA determined they are unapproved new drugs and misbranded.
GM Manufacturing is recalling 338 bottles of Longetivity Plus dietary supplements sold in California due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
GM Manufacturing is recalling 378 bottles of Chanca Piedra dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
GM Manufacturing is recalling 4,000 units of Affirm XL dietary supplements in California due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
GM Manufacturing is recalling 40,000 units of Double Mojo dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
GM Manufacturing is recalling Mega Jex capsules due to significant violations of dietary supplement cGMP regulations.
GM Manufacturing is recalling Serrapeptase, 100cc HDPE Bottles due to significant violations of current Good Manufacturing Practice (cGMP) regulations for dietary supplements.
GM Manufacturing is recalling Rinozan dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
Dermamedics, L.L.C. is recalling Calm & Correct Cream because the FDA determined the product is an unapproved new drug and misbranded.
DeRoyal is recalling Cardiac Hypothermia Trays because they contained irrigation sets previously recalled by Hospira.
Purefruit Chile S.A. is recalling Market Pantry applesauce pouches due to the possibility of mold. The product was distributed nationwide.
GM Manufacturing is recalling 188 units of Actra-SX Vinyl Bags distributed in California due to significant violations of dietary supplement cGMP regulations.
GM Manufacturing is recalling 3,404 units of Oyavon dietary supplements distributed in California due to significant violations of current Good Manufacturing Practice (cGMP) regulations.
Daiichi Sankyo is recalling specific lots of Tribenzor tablets because they were not stored at controlled room temperature during shipping.
GM Manufacturing is recalling 414 units of DMSA dietary supplements due to significant violations of current Good Manufacturing Practice (cGMP) regulations.