Verapamil recalls
The FDA has published 8 recalls involving Verapamil since 2013. The latest was reported on 17 Jul 2024. Most were for potency & assay. Amerisource Health Services has the most recalls in this group. Recalls usually affect specific lots, not every bottle on the market. Check the lot number on each recall page before acting.
Total recalls8since 2013
Last 12 months0reported
Class I00% of total
Ongoing2latest 17 Jul 2024
Recalls per month, last 24 months
click a bar for that monthSeverity split
Class I 0 0%Class II 5 63%Class III 3 38%
Why verapamil is recalled
Companies
By year
Ongoing verapamil recalls
2 active| Reported | Class | Recall | Company | Reason | Where |
|---|---|---|---|---|---|
| Drug | CLASS III | Verapamil Hydrochloride Injection, USP 10 mg/ 5 mg/mL) recalledVerapamil Hydrochloride | Zydus Pharmaceuticals (USA) | Other | Nationwide |
| Drug | CLASS III | Verapamil Hydrochloride Injection, USP 5 mg /(2.5 mg/mL) recalledVerapamil Hydrochloride | Zydus Pharmaceuticals (USA) | Packaging Defects | Nationwide |
All verapamil recalls, newest first
8 totalShould you stop taking Verapamil?
Not on your own. Most recalls affect specific lots from one manufacturer, and stopping a prescription suddenly can be riskier than the defect. Check your lot number and NDC against the recall, then call the pharmacy that dispensed it for a replacement.