Glenmark Pharmaceuticals recalls 300mg clindamycin capsules due to CGMP deviations. Affected lots have specific expiration dates. Consumers should contact the company for details.
CGMP Deviations
Glenmark Pharmaceuticals is recalling 300mg clindamycin hydrochloride capsules that were manufactured with CGMP deviations. This means the product may not meet quality standards, though the recall does not specify a risk of injury or illness.
CGMP deviations refer to failures in manufacturing quality control processes. This could mean the capsules do not meet the required standards for safety and effectiveness. However, the recall does not specify what harm this could cause.
People who own or use the recalled clindamycin capsules. Those who have the specific lot numbers and expiration dates listed in the recall are most at risk.
Check for the product name 'Clindamycin Hydrochloride Capsules, USP, 300mg, 100-count bottles'. Look for lot numbers starting with 17241278 and expiration dates of July 26, 2027.
Look for the lot number and expiration date on the bottle to confirm if it is affected.
The recall mentions CGMP deviations but does not specify a risk of injury or illness.
Check the lot number on the bottle; affected lots start with 17241278 and expire by July 26, 2027.
The recall does not provide specific action steps for consumers beyond checking product details.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0344-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0344-2025 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.