Cefdinir for Oral Suspension USP, 250 mg/5 mL, packaged in a 60 mL bottle, Rx only, Manufactured for: Lupin Pharmaceuticals…
Reason Defective container: lack of seal integrity.
Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.
Defective Container: This recall is being carried out due to the potential for improperly sealed bottles.
Cefdinir for Oral Suspension, 125 mg/5 mL, packaged in a) 60 mL bottle (NDC 0093-4136-64); b) 100 mL bottle (NDC 0093-4136-73), Rx only, Teva Pharmaceuticals USA, Sellersville, PA 18960.
What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.
Reason Defective container: lack of seal integrity.
Reason Presence of foreign substance: Product complaint of foreign material in reconstituted bottle.
Reason Presence of foreign substance: Product complaint of foreign material in reconstituted bottle.
Reason Superpotent Drug: Out-of-specification (OOS) result observed in an assay test of retention samples.
Reason Presence of Foreign substance: identified as a dead ant.
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