Glenmark Pharmaceuticals recalls 2% mupirocin ointment (22g) due to subpotent drug levels. Rx only product with specific lot numbers and expiration dates. Consumers should check their product details.
Subpotent Drug
Glenmark Pharmaceuticals is recalling mupirocin ointment 2% (22g) because it may contain lower-than-stated drug levels. This could lead to treatment being less effective for infections. The product is prescription-only and must be checked for specific lot numbers.
The ointment may have lower-than-stated drug concentration, meaning it might not effectively treat infections. This subpotency could lead to treatment failure if the product is used as intended.
Prescription patients using mupirocin ointment 2% (22g) with the listed lot numbers and expiration dates. Those with active infections requiring this medication are most at risk.
Check the product label for the lot numbers listed: 19223615, 19223537, 19223544, 19223568, 19223593, 19223641 (exp. 08/2024), and other specific lot numbers with corresponding expiration dates.
Look for the lot numbers listed in the recall notice: 19223615, 19223537, 19223544, 19223568, 19223593, 19223641, and other specific lot numbers with corresponding expiration dates.
The recall states the product may have subpotent drug levels, meaning it might not be as effective as intended. Do not use if you have the listed lot numbers.
Check the product label for the specific lot numbers listed in the recall. If you have the recalled lot numbers, contact Glenmark Pharmaceuticals for further instructions.
Look for the lot numbers: 19223615, 19223537, 19223544, 19223568, 19223593, 19223641, and other specific lot numbers with corresponding expiration dates.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0660-2024 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0660-2024 from Glenmark. 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.
