Glenmark recalls 60mg Diltiazem capsules due to potential impurity exceeding FDA limits. Affected lots expire Nov 2024-March 2025. Stop using immediately if you have these capsules.
cGMP Deviations: Presence of N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended interim limit.
Glenmark is recalling 60mg Diltiazem Hydrochloride Extended-Release Capsules because they contain an impurity that exceeds FDA safety limits. This could pose a health risk if taken as directed.
The capsules contain N-nitroso-Desmethyl-Diltiazem impurity at levels above what the FDA allows. This impurity could potentially cause health issues when taken as directed.
People with a prescription for these capsules are affected. Those who have the specific lot numbers listed in the recall are most at risk.
Check your bottle for the lot numbers: 17222544 (expires Nov 2024), 17230784 (expires March 2025), or 17231080 (expires April 2025). The product is a prescription-only 60mg capsule.
Immediately stop taking the recalled capsules if you have them.
The capsules contain N-nitroso-Desmethyl-Diltiazem impurity above FDA recommended limits.
Check the lot number on the bottle: 17222544 (expires Nov 2024), 17230784 (expires March 2025), or 17231080 (expires April 2025).
The recall record does not specify a return process.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0093-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0093-2025 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.
