Product Safety Recalls

Product Recall Tracker

LORAZEPAM Recall D-1307-2022

Description: Lorazepam Injection, USP, 2mg/mL, 1 mL vial, 25 vials per carton, RX Only, Manufactured by West-Ward Eatontown, NJ 07724, Carton NDC# 0641-6044-25, Vial NDC# 0641-6044-01

LORAZEPAM Recall D-1307-2022 Information

StatusOngoing
Mandated?Voluntary: Firm initiated
Recall NumberD-1307-2022
Event ID90583
BrandLORAZEPAM
Generic NameLORAZEPAM
ManufacturerLORAZEPAM
Original Package?1
Active SubstanceLORAZEPAM
Drug RouteINTRAMUSCULAR
DistributionNationwide in the USA
Quantity4,739,000 vials
Recall ReasonFailed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.
Drug ClassificationClass II
Drug Code Info20220817
Product NDC0641-6044 0641-6046 0641-6045
Product NUIN0000175694 M0002356
Pharma Class (EPC)Benzodiazepine [EPC]
Pharma Class (CS)Benzodiazepines [CS]
Recall Initiation Date20220711
Report Date20220817
Classification Date20220805
Address2 Esterbrook Ln
Cherry Hill, NJ 08003-4002
United States
Recalling FirmHikma Pharmaceuticals USA Inc.
Initial Notification Letter
Unique Ingredient IdentifierO26FZP769L
Drug Application NumberNDA018140
Structured Product Labeling (SPL ID)eb0543f9-51fb-4847-be6a-68d83081486c
Structured Product Labeling (SPL Set ID)e9b54e42-04cf-4c62-90e1-36f7b31a4e81
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