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.
National Enzyme Co is recalling 1.7 million Supergest bulk capsules because they may contain chloramphenicol above the 0.3 ppb limit.
National Enzyme Co is recalling bulk dietary supplement powders that may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling specific lots of Gluten & Dairy Digest enzyme supplements because they may contain chloramphenicol above 0.3 ppb.
Biomet, Inc. is recalling 21 CurvTek Eye Needles because the inner label incorrectly identifies the product size and reference number.
National Enzyme Co is recalling Wellzymes Gastric Ease enzyme supplements because a raw material may contain chloramphenicol levels above 0.3 ppb.
Nature's Way is voluntarily recalling Alive No Iron tablets because the raw material supplier reported that enzymes in the blend may contain the antibiotic chloramphenicol.
CooperVision is recalling 153 cartons of Pro Clear 1 Day Sphere contact lenses because the outer cartons display incorrect expiration dates, although the inner blisters are correct.
Qualigen Inc is recalling 17 units of the FastPack Free T4 Immunoassay because a manufacturing defect may cause lower than expected test results.
National Enzyme Co is recalling bulk enzyme powder that may contain chloramphenicol above the permitted limit.
Nature's Way is voluntarily recalling NL C 24/7 Bulk Caps because raw material enzymes may contain the antibiotic chloramphenicol.
Microgenics Corp. is recalling CEDIA Tobramycin II Assay (Lot 60169764) due to a calibration stability problem identified through two customer complaints.
A&C US Trading LLC is recalling Lam Sheng Kee Haw Flakes because the product contains unapproved food coloring. The recall affects 600 cartons distributed in New York.
National Enzyme Co is recalling 9326 Kirkman Bacterial Bio 6 dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling Bulk B199 Reviva Digestion Bulk powder because it may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling specific dietary supplements because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.
National Enzyme Co is recalling BioSan Labs Hi Potency capsules because the raw material may contain chloramphenicol above 0.3 ppb.
National Enzyme Co is recalling bulk Digest Platinum capsules because they may contain chloramphenicol above 0.3 ppb.
National Enzyme Co is recalling TriEnza digestive enzyme supplements because they may contain chloramphenicol above 0.3 ppb.
National Enzyme Co is recalling Wellzymes enzyme supplements because a raw material may contain chloramphenicol above the 0.3 ppb limit.
National Enzyme Co is recalling NWC Naturals dietary supplements because a raw material may contain chloramphenicol above 0.3 ppb.
Schwabe North America is voluntarily recalling Nature's Way Alive Once Daily MultiVitamin Ultra Potency tablets because raw material enzymes may contain the antibiotic chloramphenicol.
Schwabe North America is voluntarily recalling Nature's Way Alive Once Daily Women's 50+ probiotic tablets because raw material enzymes may contain the antibiotic chloramphenicol.
National Enzyme Co is recalling Heryben and Bulk C269 dietary supplements because they may contain chloramphenicol levels exceeding 0.3 ppb.
Stryker Neurovascular is recalling specific microcatheters and coils because they were shipped with use-by dates exceeding available shelf-life data.
National Enzyme Co is recalling bulk dietary supplement capsules because a raw material may contain chloramphenicol levels exceeding 0.3 ppb.