Zydus Pharmaceuticals (USA) Inc recalls Verapamil Hydrochloride Injection, USP 10 mg/4 mL (2.5 mg/mL), 5 x 4 mL Single-Dose Vial per carton, Rx Only, Manufactu…
- Recall date
- July 2, 2024
- Source
- U.S. Food & Drug Administration (FDA) — enforcement report
- Recall number
- D-0593-2024
- FDA classification
- Class III
- Brand / firm
- Zydus Pharmaceuticals (USA) Inc
- Sold / distributed
- Nationwide in the USA
Why it was recalled
Cross contamination with other products.
Class III means the product violates regulations but is not likely to cause harm.
What was recalled
Verapamil Hydrochloride Injection, USP 10 mg/4 mL (2.5 mg/mL), 5 x 4 mL Single-Dose Vial per carton, Rx Only, Manufactured by: Zydus Lifesciences Ltd. Vadodara, India, Distributed by: Zydus Pharmaceuticals (USA)Inc., Pennington, NJ 08534, Vial NDC: 70710-1644-1, Carton NDC: 70710-1644-5.
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