D-0574-2023 Class II Terminated

Recalled by Hikma Pharmaceuticals USA Inc. — Cherry Hill, NJ

Recall Details

Product Type
Drugs
Report Date
May 24, 2023
Initiation Date
May 11, 2023
Termination Date
December 12, 2023
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
1,352,475 vials

Product Description

Lorazepam Injection, USP, 2mg/mL, 1 mL vial (NDC 0641-6044-01), packaged in 25 x 1 mL Vials per carton (NDC 0641-6044-25), Rx only, Manufactured by West-Ward, Eatontown, NJ 07724.

Reason for Recall

Failed Impurities/Degradation Specifications: Out-of-specification results for total related compounds observed during retain steting due to the elevated Related Compound-C.

Distribution Pattern

Nationwide in the USA and Puerto Rico

Code Information

Lots: 070086, 070128, Exp. 07/2023