FDAFDA · Food and drugs·Recall number D-1308-2022
Ativan Injection (lorazepam injection, USP), 2mg/mL, 1 mL vial, 25 vials per carton, RX Only, Manufactured by West-Ward Eatontown, NJ 07724, Carton NDC# 0641-6001-25, Vial NDC# 0641-6001-01
Published August 17, 2022 · Recall initiated: July 11, 2022
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- ATIVAN
- Manufacturer
- Hikma Pharmaceuticals USA Inc.
- Distributor
- Nationwide in the USA
- Lot
- Lot # 060064Z, Exp. 06/2023
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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