Amerisource Health Services recalls 120mg Verapamil Hydrochloride Extended-Release Tablets due to failed dissolution testing. This may affect medication effectiveness. Check NDC 60687-493-01 for affected lots.
Failed Dissolution Specification: Out of specification dissolution results at time point zero. The OOS was above specified values.
Amerisource Health Services is recalling 120mg Verapamil Hydrochloride Extended-Release Tablets because they failed dissolution testing. This could mean the medication doesn't work as intended, which is serious for people needing blood pressure control.
The tablets failed a dissolution test, meaning they don't release medication properly in the body. This could lead to inconsistent blood pressure control. However, the recall is for specific lots and not all tablets.
People with prescriptions for this medication who received the recalled lot 1009065 (expiring December 31, 2023) are affected. Those with blood pressure conditions are most at risk.
Check for NDC Carton number 60687-493-01 and Lot 1009065 on the packaging. The tablets are 120mg extended-release, prescription-only, and come in 100-count cartons.
Look for NDC Carton 60687-493-01 and Lot 1009065 on the packaging.
The recall is due to failed dissolution testing, which may affect medication effectiveness. The manufacturer has not stated that taking the medication causes harm.
Check for NDC Carton 60687-493-01 and Lot 1009065 on the packaging. The tablets are 120mg extended-release, prescription-only, and come in 100-count cartons.
The recall does not specify a remedy, so contact your pharmacist or healthcare provider for guidance.
We’ve drafted a message you can send Amerisource Health Services to request your refund or repair — edit it as you like.
Subject: Recall D-0436-2023 — Amerisource Health Services Amerisource Health Services Hello, I own a Amerisource Health Services that is covered by recall D-0436-2023 from Amerisource Health Services. 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.
