Lupin Pharmaceuticals recalls Cefdinir oral suspension (250 mg/5 mL) due to foreign material complaints in reconstituted bottles. This medication is prescription-only and sold in 60mL bottles.
Presence of foreign substance: Product complaint of foreign material in reconstituted bottle.
Lupin Pharmaceuticals is recalling a prescription Cefdinir oral suspension product after reports of foreign material in reconstituted bottles. This could pose a risk if the foreign substance causes irritation or injury when taken.
The product has been reported to contain foreign material after reconstitution. This could cause irritation or injury if the foreign substance enters the mouth or throat during use.
Prescription patients who received the Cefdinir oral suspension (250 mg/5 mL) in a 60mL bottle from Lupin Pharmaceuticals. Children and elderly patients may be at higher risk due to potential irritation from foreign material.
Check for the product name 'Cefdinir for Oral Suspension USP 250 mg/5 mL (60 mL when reconstituted)' in a 60mL bottle. The product is prescription-only and manufactured by Lupin Pharmaceuticals.
Verify the product name, strength, and bottle size as described in the recall notice.
The recall is due to reports of foreign material in reconstituted bottles, but the product is generally safe if the foreign material is not present.
Check for the product name 'Cefdinir for Oral Suspension USP 250 mg/5 mL (60 mL when reconstituted)' in a 60mL bottle, which is prescription-only.
The recall notice does not specify a remedy, so contact your healthcare provider for guidance.
We’ve drafted a message you can send Lupin to request your refund or repair — edit it as you like.
Subject: Recall D-0496-2024 — Lupin Lupin Hello, I own a Lupin that is covered by recall D-0496-2024 from Lupin. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
