Glenmark recalls specific batches of Telmisartan and Hydrochlorothiazide tablets due to difficult-to-open blisters and tablet breaks. Affected lots expire by August 2023. Consumers should check product details and contact the manufacturer.
Defective Container: Recall of these batches has been initiated due to complaints of difficult to open blister and tablet breaks while opening the blister .
Glenmark is recalling certain batches of Telmisartan and Hydrochlorothiazide tablets because the blister packs are hard to open and tablets break during opening. This could lead to improper medication use if the tablets are not handled correctly.
The blister packs are difficult to open, and tablets break during opening. This could cause improper medication handling, but the hazard does not involve serious injury or death in normal use.
People who have the recalled batches of Telmisartan and Hydrochlorothiazide tablets (80 mg/12.5 mg, 30 tablets) from Glenmark. Those with prescriptions for these medications are most at risk.
Check for the product name 'Telmisartan and Hydrochlorothiazide Tablets USP, 80 mg/12.5 mg, 30 Tablets, Rx Only'. Look for lot numbers 17210929, 17210930, 17211203, 17211643, 17211646, or 17211649 with expiration dates up to August 2023.
Identify the lot number and expiration date on the packaging to determine if the product is affected.
The recall is due to complaints about difficult-to-open blister packs and tablets breaking during opening.
The official recall notice does not specify a remedy, so contact Glenmark Pharmaceuticals for further instructions.
Lots 17210929, 17210930, 17211203, 17211643, 17211646, and 17211649 with expiration dates up to August 2023.
We’ve drafted a message you can send Glenmark to request your refund or repair — edit it as you like.
Subject: Recall D-1306-2022 — Glenmark Glenmark Hello, I own a Glenmark that is covered by recall D-1306-2022 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.
