Why it was recalled
Cross contamination with other products.
Product description
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.
Lot numbers, UPCs & expiration codes
Lot L300269, Exp Date 07/31/2025
Where it was sold
Nationwide in the USA
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0593-2024
- Classification
- Class III
- Status
- Ongoing
- Recall initiated
- Jul 2, 2024
- FDA report date
- Jul 17, 2024
- Quantity
- 8020 vials
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Zydus Pharmaceuticals (USA) Inc
Original FDA data
Every field from FDA enforcement report D-0593-2024, exactly as published.
Show all FDA fields
- City
- Pennington
- State
- NJ
- Status
- Ongoing
- Country
- United States
- Event ID
- 94912
- Address
- 73 Route 31 N
- Code information
- Lot L300269, Exp Date 07/31/2025
- Postal code
- 08534-3601
- Report date
- Jul 17, 2024
- Product type
- Drugs
- Recall number
- D-0593-2024
- Classification
- Class III
- Recalling firm
- Zydus Pharmaceuticals (USA) Inc
- Product quantity
- 8020 vials
- Reason for recall
- Cross contamination with other products.
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- 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.
- Distribution pattern
- Nationwide in the USA
- Recall initiation date
- Jul 2, 2024
- Initial firm notification
- Letter
- Center classification date
- Jul 10, 2024