Home / Recalls / Hikma Pharmaceuticals USA Inc. / D-0551-2025

D-0551-2025 Class II Ongoing

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

Recall Details

Product Type
Drugs
Report Date
August 6, 2025
Initiation Date
July 22, 2025
Termination Date
N/A
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
382,775 1mL vials

Product Description

Lorazepam Injection, USP, 2 mg/mL, 25 x 1mL vials/carton, Rx Only, Manufactured by: Hikma Berkeley Heights, NJ 07922, NDC# 0641-6044-25

Reason for Recall

Failed Impurities/Degradation Specifications: An out-of-Specification for total related compounds

Distribution Pattern

Distributed Nationwide in the USA

Code Information

Lot # K24118, exp. date 10/31/2026

Other recalls by Hikma Pharmaceuticals USA Inc.

  • D-0635-2024 Class I — Acetaminophen Injection, 1,000 mg per 100 mL (10 mg/mL), 100 mL Single Dose bags (July 8, 2024)
  • D-0392-2024 Class II — Infumorph (Preservative-free Morphine Sulfate Sterile Solution), 20 mL ampul, Rx (March 12, 2024)
  • D-0574-2023 Class II — Lorazepam Injection, USP, 2mg/mL, 1 mL vial (NDC 0641-6044-01), packaged in 25 x (May 11, 2023)
  • D-0090-2023 Class II — Ganciclovir for Injection, USP, 500mg per vial, packaged in a 10-count carton, R (December 16, 2022)
  • D-1308-2022 Class II — Ativan Injection (lorazepam injection, USP), 2mg/mL, 1 mL vial, 25 vials per ca (July 11, 2022)
  • D-1307-2022 Class II — Lorazepam Injection, USP, 2mg/mL, 1 mL vial, 25 vials per carton, RX Only, Manu (July 11, 2022)
  • D-1309-2022 Class II — Lorazepam Injection, USP, 2mg/mL, 1 mL vial, 25 vial per carton, Rx Only, Novap (July 11, 2022)
  • D-1310-2022 Class II — Lorazepam Injection, USP, 4mg/mL, 1 mL vial, 25 vial per carton, Rx Only, Novap (July 11, 2022)
  • D-0771-2021 Class III — Bleomycin for Injection, USP, packaged in 15 units per single dose vial, Rx only (August 5, 2021)
  • D-0169-2021 Class II — Sodium Chloride Injection, USP, 0.9%, 0.308 mOsmol/ml, 2mL Single Dose Vial, Rx (December 7, 2020)