Hikma Pharmaceuticals recalls Lorazepam injection vials due to impurities that may cause serious harm. Affected products include 25 x 1mL vials with lot # K24118, expiring 10/31/2026. No remedy specified.
Failed Impurities/Degradation Specifications: An out-of-Specification for total related compounds
Hikma Pharmaceuticals is recalling Lorazepam injection vials because they contain impurities that could cause serious harm. This recall affects prescription-only vials manufactured in Berkeley Heights, New Jersey, with specific lot numbers and expiration dates.
The injection vials failed impurities and degradation specifications, meaning they contain harmful substances that could cause serious health issues if used. This is a quality control failure in the manufacturing process.
Prescription patients using Lorazepam injection vials with lot number K24118, expiring 10/31/2026. Healthcare providers who dispensed these vials are most at risk.
Check for vials labeled 'Lorazepam Injection, USP, 2 mg/mL, 25 x 1mL vials/carton' with lot number K24118 and expiration date 10/31/2026. These were manufactured by Hikma Berkeley Heights, NJ.
Verify the lot number and expiration date on the vial packaging to confirm if it matches the recalled batch.
The recall states the product has failed impurities and degradation specifications, so it is not safe to use. No remedy is specified in the official notice.
The official notice does not specify a remedy, so contact Hikma Pharmaceuticals for guidance on next steps.
Check for vials labeled 'Lorazepam Injection, USP, 2 mg/mL, 25 x 1mL vials/carton' with lot number K24118 and expiration date 10/31/2026.
We’ve drafted a message you can send Hikma Pharmaceuticals to request your refund or repair — edit it as you like.
Subject: Recall D-0551-2025 — Hikma Pharmaceuticals Hikma Pharmaceuticals Hello, I own a Hikma Pharmaceuticals that is covered by recall D-0551-2025 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.
