Ativan Injection recall: Impurity Out of Spec
Ativan Injection (lorazepam injection, USP), 2mg/mL, 1 mL vial, 25 vials per carton, RX Only, Manufactured by West-Ward Eatontown, NJ 07724, Carton…
Why was Ativan Injection recalled?
Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot # 060064Z, Exp. 06/2023
- Product
- Ativan Injection (lorazepam injection, USP), 2mg/mL, 1 mL vial, 25 vials per carton, RX Only, Manufactured by West-Ward Eatontown, NJ 07724, Carton…
- Recalling firm
- Hikma Pharmaceuticals USA Inc.
- Quantity
- 301,400 vials
- Distribution
- Nationwide in the USA
- Recall date
- August 17, 2022
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (drug)