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.
Aidapak Services, LLC is recalling Levothyroxine Sodium tablets due to a potential label mixup with Magnesium Chloride. The repacked drugs were distributed in four western states.
Aidapak Services is recalling Carbidopa/Levodopa tablets that may have been mislabeled as Digoxin. Patients should verify their medication labels.
Aidapak Services, LLC is recalling Losartan Potassium 50 mg tablets because they may have been mislabeled as Midodrine HCL 2.5 mg.
Remel Inc is recalling Oxoid Cefpodoxime 10 mcg. Antimicrobial Susceptibility Test Discs because some cartridges may contain discs not impregnated with antibiotic.
Aidapak Services, LLC is recalling 923 tablets of Cyanocobalamin 1000 mcg because they may have been mislabeled as other medications.
Aidapak Services, LLC is recalling 2 mg Nicotine Polacrilex Gum due to a potential labeling mixup with Folic Acid or Quetiapine Fumarate tablets.
Aidapak Services is recalling 10 mg Fosinopril Sodium tablets that may be mislabeled as Mercaptopurine 50 mg.
Aidapak Services is recalling Mycophenolate Mofetil capsules because they may have been mislabeled as Atorvastatin or Propranolol.
Aidapak Services is recalling Losartan Potassium 50 mg tablets because they may have been mislabeled as Atorvastatin Calcium 80 mg.
Davol, Inc. is recalling 46 units of Composix L/P Mesh with Echo PS Positioning System because the product labeling does not match the product configuration.
Aidapak Services, LLC is recalling Triamterene/HCTZ tablets that may have been mislabeled as Caffeine tablets. The error involves a label mixup during repacking.
KVK-Tech, Inc. is recalling 14,664 bottles of Hydroxyzine Hydrochloride 10 mg tablets because the active ingredient came from an unapproved source.
Aidapak Services is recalling Verapamil HCL tablets because they may have been mislabeled as Atorvastatin or Tacrolimus.
Aidapak Services, LLC is recalling Nortriptyline HCL capsules because they may have been mislabeled as other medications. The affected drugs were distributed in four western states.
Aidapak Services, LLC is recalling CapsuleTOPRIL tablets because they may have been mislabeled as Calcitriol capsules. The error could lead to patients receiving the wrong medication.
Remel Inc is recalling Oxoid Ertapenem 10 mcg. Antimicrobial Susceptibility Test Discs because some cartridges may contain discs not impregnated with antibiotic.
Aidapak Services, LLC is recalling 5 mcg Liothyronine Sodium tablets because they may have been mislabeled as 25 mcg tablets.
Aidapak Services, LLC is recalling Dronedarone HCL 400 mg tablets because they may be mislabeled as Methylergonovine Maleate 0.2 mg.
Aidapak Services is recalling Repaglinide 1 mg tablets because they may have been mislabeled as Valsartan, Guaifenesin, or Magnesium Chloride.
Aidapak Services, LLC is recalling Propranolol HCL ER capsules because they may have been mislabeled as Cinacalcet HCL tablets.
Aidapak Services, LLC is recalling Oxybutynin Chloride 5 mg tablets because they may have been mislabeled as other prescription drugs.
Aidapak Services is recalling Nefazodone HCL 150 mg tablets because they may have been mislabeled as Liothyronine Sodium 25 mcg.
Aidapak Services, LLC is recalling Hydrochlorothiazide 12.5 mg tablets because they may have been mislabeled as other prescription drugs.
Ortho-Clinical Diagnostics is recalling VITROS Chemistry Products COCM Reagent because of inaccurate quality control results. The recall affects 3,342 units distributed worldwide.
Aidapak Services is recalling Thiothixene 1 mg capsules because they may have been mislabeled as Omega-3 Fatty Acid 1000 mg capsules.