Lupin Pharmaceuticals recalls Cefdinir oral suspension 250mg/5mL (60mL bottle) due to container seal failure. Rx-only medication may leak or contaminate. Contact for return instructions.
Defective container: lack of seal integrity.
Lupin Pharmaceuticals is recalling a specific prescription antibiotic (Cefdinir oral suspension) because its container may not seal properly. This could lead to medication leakage or contamination, which might affect treatment effectiveness.
The container lacks proper seal integrity, which could allow the medication to leak or become contaminated. This might reduce the effectiveness of the antibiotic or cause unintended exposure to contaminants.
Prescription patients who received this specific Cefdinir oral suspension (250 mg/5 mL, 60 mL bottle) from Lupin. Those with the medication at risk of potential leakage or contamination.
Check for the Cefdinir oral suspension 250 mg/5 mL in a 60 mL bottle, manufactured by Lupin Pharmaceuticals. The product was sold with lot numbers F305184, F305185, or F305186 and expires July 31, 2025.
Verify the product contains Cefdinir oral suspension 250 mg/5 mL in a 60 mL bottle with lot numbers F305184, F305185, or F305186.
The recall is due to potential container leaks or contamination, but the medication itself is safe if the container seals properly. Consult your healthcare provider for guidance.
Check for the Cefdinir oral suspension 250 mg/5 mL in a 60 mL bottle with lot numbers F305184, F305185, or F305186.
The recall record does not specify a remedy, so contact Lupin Pharmaceuticals directly for instructions on handling the product.
We’ve drafted a message you can send Lupin to request your refund or repair — edit it as you like.
Subject: Recall D-0518-2024 — Lupin Lupin Hello, I own a Lupin that is covered by recall D-0518-2024 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.
