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.
US Pharmaceuticals is recalling CVS Therapeutic Menthol Gel because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
American Health Packaging is recalling Carbamazepine Extended-Release Tablets, 400 mg, because they failed to meet dissolution specifications.
US Pharmaceuticals is recalling CVS Health Glycerin Suppositories because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
Zimmer Biomet is recalling 39 units of the Orthopedic Salvage System Hybrid Poly Tibia due to potentially ineffective cleaning processes.
Kerry, Inc. is recalling 712 bags of CFS Breader 35% RDC SOD due to the presence of foreign material, specifically nylon string.
Zimmer Biomet is recalling 19 units of Orthopedic Salvage System Hybrid Poly Tibia components because cleaning processes may be ineffective.
Macleods Pharma USA Inc is recalling Tamsulosin Hydrochloride Capsules because they failed to meet dissolution specifications.
Alvogen, Inc. is recalling 2,784 bottles of Nitrofurantoin Monohydrate/Macrocrystalline capsules because they failed to meet dissolution specifications.
US Pharmaceuticals Inc. is recalling 305 cases of Maximum Strength Hydrocortisone Cream because the purified water used in manufacturing failed quality tests.
Kerry, Inc. is recalling 564 bags of Batter Mix due to the presence of nylon string. The product was distributed to manufacturers and food service distributors in nine US states.
Kerry, Inc. is recalling 1,470 bags of Breader containing nylon string. The product was distributed to manufacturers and food service distributors in nine states.
Kerry, Inc. is recalling 309 bags of Breader W/Soy due to the presence of nylon string. The product was distributed to manufacturers and food service distributors in nine US states.
Kerry, Inc. is recalling 176 bags of 50 lb Batter Mix because the product contains nylon string. The product was distributed to manufacturers and food service distributors in nine US states.
Kerry, Inc. is recalling 105 bags of Breader containing nylon string. The product was distributed to manufacturers and food service distributors in nine states.
Kerry, Inc. is recalling 51 bags of Batter Mix due to the presence of nylon string. The product was distributed to manufacturers and food service distributors in nine US states.
Kerry, Inc. is recalling 52 bags of Batter Mix due to the presence of nylon string. The product was distributed to manufacturers and food service distributors in nine US states.
Kerry, Inc. is recalling 210 bags of Ultimate Batter/Breader due to the presence of nylon string. The product was distributed to manufacturers and food service distributors in nine US states.
US Pharmaceuticals is recalling 76 cases of Children Glycerin Suppositories due to out-of-specification results in the purified water used during manufacturing.
Kerry, Inc. is recalling 102 bags of Italian Chicken Breader because the product contains foreign material, specifically nylon string.
Luminex is recalling ARIES Group A Strep Assay kits because side cassette seals may not meet specifications, potentially affecting test sensitivity and stability.
Kerry, Inc. is recalling 157 bags of Batter Mix 20% RDC SOD due to the presence of nylon string. The product was distributed to manufacturers and food service distributors in nine US states.
Kerry, Inc. is recalling 826 bags of Breader with Crushed Cracker due to the presence of nylon string. The product was distributed to manufacturers and food service distributors in nine US states.
Kerry, Inc. is recalling 308 bags of Italian CKN Batter Mix due to the presence of nylon string. The product was distributed to manufacturers and food service distributors in nine states.
US Pharmaceuticals is recalling CVS Health Glycerin Suppositories due to out-of-specification results for microbial count or organic carbon in the purified water used during manufacturing.
US Pharmaceuticals is recalling 830 tubes of Soothe&Cool Protect Moisture Guard Skin Protectant due to out-of-specification results for microbial count or organic carbon in purified water.