Glenmark Pharmaceuticals recalls 325mg extended-release capsules due to manufacturing deviations. This may affect safety in normal use. Check NDC# 16714-826-01 and lot # 17230767 for affected products.
CGMP Deviations
Glenmark Pharmaceuticals is recalling 325mg extended-release propafenone capsules that were manufactured with CGMP deviations. This recall is due to potential safety risks from improper manufacturing processes.
CGMP deviations refer to manufacturing process failures that could lead to unsafe product quality. This recall is initiated because the product may not meet the required safety standards for prescription use.
Prescription users of the 325mg extended-release propafenone capsules. Those who have the specific NDC# 16714-826-01 lot # 17230767 bottles are most at risk.
Check for NDC# 16714-826-01 and lot # 17230767 on the bottle. The product is a 325mg extended-release capsule, 60-count bottle, prescription-only.
Look for NDC# 16714-826-01 and lot # 17230767 on the bottle label.
The recall is due to CGMP deviations, which may affect safety. The product is not safe to use as it was manufactured with potential quality issues.
Check the NDC# 16714-826-01 and lot # 17230767 on the bottle label.
The recall 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-0352-2025 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-0352-2025 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.
