RecallDepth
Class I Terminated

Acyclovir Sodium Injection 1000mg/20mL (50mg/mL) vial NDC 68382-049-01, For Intravenous Infusion Only MUST BE DILUTED PRIOR TO USE, packaged in 10 x 20mL Single-Dose Vials per pack NDC 68382-049-10, Rx only, Manufactured by: Cadila Healthcare Ltd., Vadodara, India. Distributed by: Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534.

This recall has been terminated (originally issued April 7, 2021).

Company
Zydus Pharmaceuticals (Usa) Inc
Recall Initiated
February 18, 2021
Posted
April 7, 2021
Recall Number
D-0315-2021
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
816 packs
Firm Location
Pennington, NJ, United States
Official Source
View on FDA website ↗

Reason for Recall

Crystallization: customer complaints for crystallization in finished product.

Distribution

USA Nationwide

Lot / Code Info

Lot#: L000155, Exp 12/2021; L000156, Exp 1/2022

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