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.
Greiner Bio-One is recalling VACUETTE 2mL 9NC Coagulation Tubes because the sodium citrate anticoagulant levels were inconsistent. The recall affects 1,000,800 units distributed nationwide.
The Medicine Shoppe Pharmacy in Port Charlotte, FL, is recalling Paregoric Compound Solution due to a lack of processing control.
Filltech USA is recalling Dermatone Sunscreen Lotion SPF 50 due to positive tests for yeast and bacteria.
The Medicine Shoppe Pharmacy is recalling Naltrexone 4.5 mg capsules due to a lack of processing control.
The Medicine Shoppe Pharmacy is recalling Bi-Est 8:2/Progesterone/Testosterone DHEA capsules due to lack of processing control.
The Medicine Shoppe Pharmacy in Port Charlotte, FL, is recalling Bi-Est cream due to a lack of processing control. The affected product is a prescription topical cream.
The Medicine Shoppe Pharmacy is recalling Bi-Est (1:1)/Progesterone/Testosterone cream due to a lack of processing control. The affected product is distributed in Florida.
Herbal Doctor Remedies is recalling DeTensin Ex because the product is misbranded as an unapproved new drug. The recall covers all lots within expiry sold in the US and internationally.
Herbal Doctor Remedies is recalling Phlegm Off capsules because the products are misbranded as unapproved new drugs.
Biomet, Inc. is recalling BIOMET StageOne Knee Femoral Cement Spacer Molds because the cleaning process may have been insufficient or inadequately monitored.
Herbal Doctor Remedies is recalling Lupus Care because the product is misbranded as an unapproved new drug. The product was sold online in the US and internationally.
Herbal Doctor Remedies is recalling Sweat Oil because it is misbranded as an unapproved new drug. The product was sold online in the US and internationally.
Herbal Doctor Remedies is recalling Herpes V Balm because the product was found to be misbranded as an unapproved new drug.
Biomet, Inc. is recalling 230,001 units of StageOne Select Hip Stem Cement Spacer Molds due to potentially insufficient cleaning processes.
Biomet is recalling 230,001 units of StageOne Hip Cement Spacer Molds because of potentially insufficient cleaning processes or inadequate monitoring of cleaning parameters.
Biomet, Inc. is recalling StageOne Hip Cement Spacer Molds because of a potentially insufficient cleaning process or inadequate monitoring of cleaning parameters.
Biomet is recalling 230,001 units of StageOne Shoulder Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring.
Herbal Doctor Remedies is recalling Herpes-G 500mg capsules because they are misbranded as unapproved new drugs.
Herbal Doctor Remedies is recalling Blood Clot Purger because the product is misbranded as an unapproved new drug.
Herbal Doctor Remedies is recalling Age Stop Ex because the product is misbranded as an unapproved new drug.
Herbal Doctor Remedies is recalling Skin Lift because the product is misbranded as an unapproved new drug.
Herbal Doctor Remedies is recalling Edema Off because the product was found to be misbranded as an unapproved new drug due to CGMP deviations.
Herbal Doctor Remedies is recalling BioMycin 500mg capsules because they are misbranded as unapproved new drugs.
Herbal Doctor Remedies is recalling Thyro-Lo 500mg capsules because they are misbranded as unapproved new drugs. The products were sold online in the US and internationally.
Biomet, Inc. is recalling specific lots of StageOne Select Hip Stem Cement Spacer Molds due to potentially insufficient cleaning processes or inadequate monitoring.