Lupin Pharmaceuticals recalls 100mg/5mL oral suspension bottles due to failed impurities and degradation specifications. This prescription drug may pose safety risks if used as intended.
Failed Impurities/Degradation Specifications
Lupin Pharmaceuticals is recalling a specific prescription cefixime oral suspension product because it failed impurities and degradation tests. This could mean the medication might not be safe to use as intended, though the exact risk level isn't clearly described in the recall.
The product failed impurities and degradation specifications, meaning it may contain harmful substances or break down in a way that could affect safety. However, the recall does not specify how this could cause harm in normal use.
Prescription patients who received this specific cefixime oral suspension product (100mg/5mL, 50mL bottle) from Lupin Pharmaceuticals. Those with the product's lot number F304833 are most at risk.
Check for the product name 'Cefixime for Oral Suspension 100mg/5mL', 50mL bottle, prescription-only, with lot number F304833 manufactured by Lupin Pharmaceuticals Inc. in Baltimore, Maryland.
Verify the product's lot number (F304833) and expiration date (06/2025) to confirm if it's recalled.
The recall states the product failed impurities and degradation specifications, but does not specify if it's safe to use. The manufacturer has not provided details on the exact risk.
The recall does not specify a remedy or action for affected products. You should check the product details to confirm if it's recalled.
The recall record does not mention any replacement or remedy options.
We’ve drafted a message you can send Lupin Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0274-2024 — Lupin Pharmaceuticals Lupin Pharmaceuticals Hello, I own a Lupin Pharmaceuticals that is covered by recall D-0274-2024 from Lupin Pharmaceuticals. 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.
