Amneal recalls prescription oseltamivir suspension due to failed impurities tests. This may cause health risks. Check NDC# 69238-1273-6 or lot numbers for affected products.
Failed Impurities/Degradation Specifications: Out-of-specification test results.
Amneal is recalling prescription oseltamivir suspension bottles that failed impurities tests. This could pose health risks to users, so affected individuals should check their product details.
The suspension failed impurities and degradation tests, meaning it may contain harmful substances. This could lead to health issues if used as intended.
Prescription patients using the recalled oseltamivir suspension. Those with the specific NDC number or lot numbers listed are most at risk.
Check for NDC# 69238-1273-6 or lot numbers BF22722A (exp. 08/31/2024) or BJ15122A (exp. 09/30/2024). The product is prescription-only and distributed by Amneal.
Look for NDC# 69238-1273-6 or lot numbers BF22722A or BJ15122A on the bottle.
The recall states the product failed impurities tests, so it may contain harmful substances. Do not use it.
The recall does not specify a remedy, so check with your healthcare provider for guidance.
Check the NDC# 69238-1273-6 or lot numbers BF22722A or BJ15122A on the bottle.
We’ve drafted a message you can send Amneal to request your refund or repair — edit it as you like.
Subject: Recall D-0327-2024 — Amneal Amneal Hello, I own a Amneal that is covered by recall D-0327-2024 from Amneal. 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.
