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 Propranolol HCL 10 mg tablets because they may be mislabeled as Lactobacillus Acidophilus capsules.
Aidapak Services is recalling Galantamine HBR ER capsules due to a potential label mixup with Escitalopram tablets.
Aidapak Services is recalling Multivitamin/Multimineral Tablets due to a labeling error where they may be mislabeled as Prenatal Multivitamin/Multimineral Tablets.
Aidapak Services is recalling Desipramine HCL tablets that may be mislabeled as clomipramine HCl capsules due to a label mixup.
Aidapak Services is recalling Multivitamin/Multimineral tablets that may be mislabeled as Omega-3 or Guaifenesin products.
GE Healthcare is recalling Centricity PACS System versions 3.X and 4.X due to a potential loss of diagnostic images during transfers between servers.
Aidapak Services, LLC is recalling Phenobarbital/Hyoscyamine/Atropine/Scopolamine tablets because they may be mislabeled as Valsartan. The repacked drugs were distributed in four western states.
Aidapak Services, LLC is recalling Metaxalone 800 mg tablets because they may be mislabeled as Esterified Estrogens 0.625 mg.
Aidapak Services is recalling Phytonadione 5 mg tablets because they may be mislabeled as other prescription drugs. The affected repacked drugs were distributed in four western states.
Aidapak Services, LLC is recalling Magnesium Chloride tablets because they may be mislabeled as other medications. The repacked drugs were distributed in four western states.
Leica Biosystems is recalling BOND Polymer Refine Red Detection kits because they may contain fungal contaminants that can cause staining sensitivity loss or fluid delivery obstructions.
Aidapak Services, LLC is recalling Calcitriol 0.5 mcg capsules because they may be mislabeled as Niacin or Isoniazid. The repacked drugs were distributed in four western states.
Aidapak Services, LLC is recalling Doxycycline Hyclate 100 mg tablets because they may be mislabeled as Desloratadine 5 mg tablets.
Aidapak Services, LLC is recalling 1 mg Glimepiride tablets because they may be mislabeled as Clomipramine HCl capsules.
Aidapak Services, LLC is recalling Vitamin B Complex Prolonged Release tablets because they may be mislabeled as guaiFENesin ER or tolterodine tartrate ER.
Aidapak Services is recalling Lisinopril 2.5 mg tablets because they may be mislabeled as Ranolazine ER or Docusate Sodium.
Aidapak Services, LLC is recalling Pancrelipase DR capsules because they may be mislabeled as Melatonin or Verapamil HCL. The repacked drugs were distributed in four western states.
Aidapak Services is recalling Nitrofurantoin capsules that may be mislabeled as Minocycline. The error could lead to patients receiving the wrong medication.
Aidapak Services, LLC is recalling Acarbose 25 mg tablets because they may be mislabeled as Lactobacillus GG capsules.
Aidapak Services, LLC is recalling Modafinil 50 mg tablets that may be mislabeled as Saccharomyces boulardii capsules due to a labeling mixup.
Aidapak Services, LLC is recalling Atorvastatin Calcium 20 mg tablets because they may be mislabeled as GuaiFENesin ER 600 mg.
Aidapak Services, LLC is recalling Omega-3 Fatty Acid capsules because they may be mislabeled as tizanidine HCL tablets.
Aidapak Services, LLC is recalling Orphenadrine Citrate ER tablets because they may be mislabeled as Omega-3 Fatty Acid capsules.
Aidapak Services, LLC is recalling buPROPion HCl ER 200 mg tablets because they may be mislabeled as amantadine HCl 100 mg capsules.
Aidapak Services is recalling Warfarin Sodium 0.5 mg tablets that may be mislabeled as Sodium Chloride 1 mg tablets.