Harvard Drug Group recalls methylergonovine maleate tablets (0.2 mg) with subpotent drug risk. Affected lots expire 09/2026 to 08/2027. Consumers should contact the manufacturer for details.
Subpotent Drug
Harvard Drug Group is recalling methylergonovine maleate tablets (0.2 mg) because they may be subpotent. This means the medication might not work as intended, which could lead to ineffective treatment for conditions like postpartum hemorrhage.
Subpotent drugs do not contain the full amount of active ingredient needed for the intended effect. This could result in the medication being less effective than prescribed, potentially leading to inadequate treatment for conditions such as postpartum hemorrhage.
People who have the recalled methylergonovine maleate tablets (0.2 mg) with specific lot numbers. Healthcare providers and patients using these tablets for medical purposes are most at risk.
Check the blister label for the product name 'Methylergonovine Maleate Tablets, 0.2 mg, USP'. Look for lot numbers N02327 (expires 09/2026), N02740 (expires 12/2026), or N03069 (expires 08/2027).
Identify the lot number on the blister label to confirm if your tablets are in the recalled lots.
Reach out to Harvard Drug Group for specific instructions on what to do with the recalled tablets.
The medication may be subpotent, meaning it contains less active ingredient than labeled, which could lead to ineffective treatment.
Recalled lots include N02327 (expires 09/2026), N02740 (expires 12/2026), and N03069 (expires 08/2027).
The recall does not specify a stop-use instruction; contact Harvard Drug Group for specific guidance.
We’ve drafted a message you can send The Harvard Drug Group to request your refund or repair — edit it as you like.
Subject: Recall D-0609-2026 — The Harvard Drug Group The Harvard Drug Group Hello, I own a The Harvard Drug Group that is covered by recall D-0609-2026 from The Harvard Drug Group. 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.
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