Amneal recalls 0.2mg methylergonovine maleate tablets with failed dissolution specs. This may affect medication effectiveness. Check NDC #69238-1605-2 and lot BJ01922A for affected products.
Failed Dissolution Specifications
Amneal is recalling 0.2mg methylergonovine maleate tablets that failed dissolution tests. This could mean the medication doesn't work properly when taken as directed.
The tablets failed dissolution specifications, meaning they may not release the medication properly in the body. This could lead to ineffective treatment if the medication doesn't work as intended.
People prescribed methylergonovine maleate for medical use who have the specific 12-count bottle with NDC #69238-1605-2 and lot BJ01922A. Those with the product are most at risk.
Check for the 12-count bottle labeled 'Methylergonovine Maleate Tablets, USP, 0.2mg' with NDC #69238-1605-2 and lot number BJ01922A. The expiration date is March 2024.
Verify the NDC number (69238-1605-2) and lot number (BJ01922A) on the bottle.
The recall is for failed dissolution specifications, which may affect medication effectiveness. The product is not safe to use as intended.
The recall record does not specify a remedy, so check with your healthcare provider for guidance.
Look for the NDC number 69238-1605-2 and lot number BJ01922A on the bottle label.
We’ve drafted a message you can send Amneal to request your refund or repair — edit it as you like.
Subject: Recall D-0477-2024 — Amneal Amneal Hello, I own a Amneal that is covered by recall D-0477-2024 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.
