Key Takeaway

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. by Hikma Pharmaceuticals USA Inc. was recalled on May 11, 2023. The hazard: Failed Impurities/Degradation Specifications: Out-of-specification results for total related compounds observed during retain steting due to the eleva...

FDA Drug Class II Terminated

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.

Recalled: May 11, 2023 ~1,352,475 vials units affected D-0574-2023

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.

Hazard / Reason

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

Class II: Product that may cause temporary or medically reversible health consequences.

Class II indicates the product may cause temporary or medically reversible health effects. The probability of serious harm is considered remote.

Products Affected

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.

Drugs

Company Information

Hikma Pharmaceuticals USA Inc.

Cherry Hill, NJ, United States

View all 18 recalls by Hikma Pharmaceuticals USA Inc. →

Distribution

Nationwide in the USA and Puerto Rico

Related Recalls

Frequently Asked Questions

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