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.
Becton Dickinson is recalling 176 units of BD MAX MRSA Reagent Kits because foil bags containing extraction tubes may not have been sealed properly.
US Pharmaceuticals is recalling 98 cases of Walgreens Adult Glycerin Suppositories due to out-of-specification results in the purified water used during manufacturing.
Kerry, Inc. is recalling 310 bags of Hot N Spicy Breader because the product contains foreign material, specifically nylon string.
Kerry, Inc. is recalling Pork Fritter 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 Kool Comfort Cooling Pain Relief because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
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 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 CVS Therapeutic Menthol Gel because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
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 103 bags of Scallopini Batter because the product contains foreign material, specifically nylon string. The product was distributed to manufacturers and food service distributors in nine US states.
Kerry, Inc. is recalling Sweet Onion Crusted Batter due to the presence of nylon string. The product was distributed to manufacturers and food service distributors in nine US states.
Suntech Medical is recalling 80 neonate blood pressure cuffs because size #3 cuffs were packaged with size #4 labels.
Codman & Shurtleff Inc is recalling 28 units of the Galaxy G3 Mini Microcoil Delivery System because the label displays the incorrect coil length.
US Pharmaceuticals is recalling Intensive Healing Eczema Lotion due to out-of-specification results for microbial count or organic carbon in the purified water used during manufacturing.
Kerry, Inc. is recalling 154 bags of Breader (Item 30753219.49) because the product contains foreign material, specifically nylon string.
US Pharmaceuticals is recalling 246 cases of Cool Hot Ice Analgesic Gel because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
Kerry, Inc. is recalling 52 bags of Breader (Item 30753324.49) because the product contains 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 642 bags of CFS Breader because the product contains foreign material (nylon string). The product was distributed to manufacturers and food service distributors in nine US 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.
US Pharmaceuticals is recalling 651 cases of Maximum Strength Hydrocortisone Cream because the purified water used in manufacturing failed quality tests for microbial count or organic carbon.
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 310 bags of Batter Mix due to the presence of nylon string. The product was distributed to manufacturers and food service distributors in nine states.
Kerry, Inc. is recalling Conch Fritter Mix because it contains nylon string. The product was distributed to manufacturers and food service distributors in nine US states.
US Pharmaceuticals is recalling specific lots of Maximum Strength Hydrocortisone Cream with Aloe because the purified water used in manufacturing failed quality tests.