RemedyRepack recalls LORazepam 2mg/mL injection vials due to quality program discontinuation. Affected lots expire 2023-2025. Contact for remedy details.
CGMP Deviations: Discontinuation of the Quality program by manufacturer that would assure product meet the identity, strength, quality, and purity characteristics that they are purported or represented to possess.
RemedyRepack is recalling specific lots of LORazepam injection vials because the manufacturer stopped their quality assurance program. This could mean the medication doesn't meet safety standards. Patients using these vials should stop using them and contact their healthcare provider.
The manufacturer discontinued their quality program, which means the product may not meet the required safety and purity standards. This could lead to medication that isn't effective or has harmful impurities.
Prescription patients using the recalled LORazepam injection vials. Those with the specific lot numbers listed in the recall are most at risk.
Check the vial label for the product name 'LORazepam Injection, 2mg/mL Single Dose vial 1ml vial, Rx Only'. Look for the lot numbers listed in the recall (e.g., B2169656-032223) and expiration dates between January 2023 and April 2025.
Immediately stop using the recalled LORazepam injection vials if you have them.
The manufacturer discontinued their quality assurance program, which could mean the product doesn't meet safety and purity standards.
Stop using the vials immediately and contact your healthcare provider for instructions.
Check the vial label for the product name and lot numbers listed in the recall (e.g., B2169656-032223).
We’ve drafted a message you can send RemedyRepack to request your refund or repair — edit it as you like.
Subject: Recall D-0576-2023 — RemedyRepack RemedyRepack Hello, I own a RemedyRepack that is covered by recall D-0576-2023 from RemedyRepack. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
