Hikma Pharmaceuticals recalls Ativan injection due to failed impurities testing. This medication may contain harmful substances that could cause health issues. Affected lots: Lot #060064Z, Exp. 06/2023.
Failed Impurities/Degradation Specifications: Out-of-specification results observed for total related compounds during testing of retain samples.
Hikma Pharmaceuticals is recalling Ativan injection (lorazepam) vials that may contain harmful impurities. This could pose health risks to patients using the medication as prescribed.
The medication failed impurities testing, meaning it may contain harmful substances. This could lead to health issues if the injection is used as intended.
Patients prescribed Ativan injection by a doctor are affected. Those using the recalled lot numbers are at risk.
Check for the carton NDC# 0641-6001-25 and vial NDC# 0641-6001-01. The affected lot number is 060064Z, with an expiration date of 06/2023.
Look for the carton NDC# 0641-6001-25 and vial NDC# 0641-6001-01 on the packaging.
The recall indicates the product may contain harmful impurities, so it is not safe to use as recalled.
The official recall does not specify a remedy, so contact Hikma Pharmaceuticals for guidance.
The recalled product expires on 06/2023 (June 2023).
We’ve drafted a message you can send Hikma Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-1308-2022 — Hikma Pharmaceuticals Hikma Pharmaceuticals Hello, I own a Hikma Pharmaceuticals that is covered by recall D-1308-2022 from Hikma Pharmaceuticals. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
