Verapamil Hydrochloride recalls

Verapamil Hydrochloride products have been recalled 3 times, most recently on 17 Jul 2024. The recalling company is usually Zydus Pharmaceuticals (USA). The most common reason is packaging defects.

Total recalls3since 2021
Last 12 months0reported
Class I00% of total
Ongoing2latest 17 Jul 2024

Recalls per month, last 24 months

click a bar for that month

Severity split

Class I 0 0%Class II 1 33%Class III 2 67%

Why verapamil hydrochloride is recalled

Product types

By year

Ongoing verapamil hydrochloride recalls

2 active
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIIVerapamil Hydrochloride Injection, USP 10 mg/ 5 mg/mL) recalledVerapamil HydrochlorideZydus Pharmaceuticals (USA)OtherNationwide
DrugCLASS IIIVerapamil Hydrochloride Injection, USP 5 mg /(2.5 mg/mL) recalledVerapamil HydrochlorideZydus Pharmaceuticals (USA)Packaging DefectsNationwide

All verapamil hydrochloride recalls, newest first

3 total
ReportedClassRecallCompanyReasonWhere
DrugCLASS IIIVerapamil Hydrochloride Injection, USP 10 mg/ 5 mg/mL) recalledVerapamil HydrochlorideZydus Pharmaceuticals (USA)OtherNationwide
DrugCLASS IIIVerapamil Hydrochloride Injection, USP 5 mg /(2.5 mg/mL) recalledVerapamil HydrochlorideZydus Pharmaceuticals (USA)Packaging DefectsNationwide
DrugCLASS IIVerapamil Hydrochloride Extended-Release Tablets USP 120 mg recalledVerapamil HydrochlorideCardinal HealthManufacturing (CGMP) DeviationsFL, GA, SC

About this list

Records come from FDA enforcement reports and USDA FSIS notices, grouped by normalised name. A company operating under several names may appear more than once.