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.
Wilton Brands is recalling 14,943 bottles of Green Airbrush Color due to the potential for contamination with mold, yeast, or bacteria.
Wilton Brands is recalling 17,670 bottles of Silver Airbrush Color found to contain mold, yeast, or bacteria. The product was distributed nationwide in the U.S. and Canada.
Zimmer Biomet is recalling 703 Patellofemoral Joint Prosthesis Milling Handpieces because they may be inoperable due to lack of preventative maintenance, potentially delaying surgery.
Pharmatech LLC is recalling 6,024 bottles of Pedia Tri-Vite Drops with Iron as a precautionary measure due to potential contamination with Burkholderia cepacia.
Pharmatech LLC is recalling 48,024 bottles of Liquid Vitamin C due to a precautionary measure regarding potential contamination with Burkholderia cepacia.
Pharmatech LLC is recalling Poly-Vita Drops dietary supplements due to a precautionary measure regarding potential contamination with Burkholderia cepacia.
Pharmatech LLC is recalling Poly-Vita Drops with Iron as a precaution due to potential contamination with Burkholderia cepacia.
Pharmatech LLC is recalling 6,048 bottles of Calcionate Syrup as a precautionary measure due to potential contamination with Burkholderia cepacia.
Wilton Brands is recalling 14,595 bottles of Purple Airbrush Color due to potential contamination with mold, yeast, or bacteria.
Pharmatech LLC is recalling Tri-Vitamin dietary supplement bottles due to a precautionary measure regarding potential Burkholderia cepacia contamination.
Keystone Dental Inc. is recalling 55 units of PrimaConnex Straight Implants because small diameter cover screws were packaged with regular diameter implants.
Pharmatech LLC is recalling 8,232 bottles of Virtrate-K dietary supplement due to a precautionary measure regarding potential Burkholderia cepacia contamination.
TZ Medical is recalling Neptune Plus hemostatic pads because the labels incorrectly state they include an antimicrobial barrier.
Pharmatech LLC is recalling Tri-Vita Drops dietary supplements due to a precautionary measure regarding potential contamination with Burkholderia cepacia.
Wilton Brands is recalling 11,103 bottles of Brown Airbrush Color due to the potential for contamination with mold, yeast, or bacteria.
Wilton Brands is recalling Red Airbrush Color due to the potential for contamination with mold, yeast, or bacteria.
Pharmatech LLC is recalling Renew HC dietary supplement bottles due to a precautionary measure regarding potential contamination with Burkholderia cepacia.
Pharmatech LLC is recalling Polyvitamin Liquid as a precautionary measure due to potential contamination with Burkholderia cepacia. The product was distributed in Florida, Michigan, Mississippi, and Ohio.
Pharmatech LLC is recalling 31,224 bottles of Ferrous Drops dietary supplements due to a precautionary measure regarding potential contamination with Burkholderia cepacia.
Pharmatech LLC is recalling Pedia D-Vite Drops as a precaution due to potential contamination with Burkholderia cepacia.
Pharmatech LLC is recalling 129,268 bottles of Cerovite Liquid dietary supplement due to a precautionary measure regarding potential contamination with Burkholderia cepacia.
Pharmatech LLC is recalling 8,712 bottles of Pedia Tri-Vite Drops due to a potential risk of contamination with Burkholderia cepacia.
Siemens Healthcare Diagnostics is recalling IMMULITE CMV IgM Assay kits due to reported increases in imprecision and high coefficient of variation (CV) values.
Bob's Red Mill is voluntarily recalling one lot of Guar Gum due to the inclusion of a misidentified ingredient, hydroxyethylcellulose.
Pharmatech LLC is recalling 99,024 bottles of Fer-Iron Liquid dietary supplement as a precautionary measure due to potential contamination with Burkholderia cepacia.