Glenmark recalls 120mg Diltiazem capsules due to failed dissolution specifications. Rx-only medication may not release properly in the body. Contact for return instructions.
Failed Dissolution Specifications
Glenmark is recalling 120mg Diltiazem Hydrochloride Extended-Release Capsules because they failed dissolution tests. This means the medication might not work properly in your body, which could affect blood pressure control.
The capsules failed dissolution specifications, meaning they may not release the medication properly in the body. This could lead to inconsistent blood pressure control. However, the recall is for a specific batch and not all Diltiazem products.
People with prescribed blood pressure treatment using this specific capsule formulation. Those who have been prescribed this medication by their doctor are most at risk.
Check for the product name 'Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, Twice-a-Day Dosage, 100 Capsules per bottle, Rx Only'. Look for the lot number 17221312 and expiration date 5/31/2024.
Verify the product name, lot number 17221312, and expiration date 5/31/2024 on the bottle.
The recall is for a specific batch that failed dissolution tests. Other batches may be safe, but this particular product should not be used.
Check for the product name 'Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, Twice-a-Day Dosage, 100 Capsules per bottle, Rx Only' with lot number 17221312 and expiration date 5/31/2024.
The recall record does not specify a remedy, so contact your doctor or pharmacist for guidance.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-0472-2024 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0472-2024 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
