Olympia Pharmacy recalls QM-2 vials with CGMP deviations from October 2021. These multi-dose vials may have uninvestigated monitoring issues. Affected vials have specific NDC and lot numbers.
CGMP Deviations: prior to October 1, 2021, environmental and personnel monitoring Out of Action Limit (OOAL) excursions were not being properly investigated
Olympia Pharmacy is recalling QM-2 multi-dose vials that were produced before October 2021 due to improper investigation of environmental and personnel monitoring failures. This could lead to unsafe drug concentrations if not properly managed.
The vials were produced before October 2021 and had uninvestigated monitoring issues. This means environmental and personnel safety checks might not have been properly addressed, potentially leading to unsafe drug concentrations.
Prescription patients who received QM-2 vials with NDC 73198-0018-10 and lots D41219 or I24C13. Healthcare providers using these vials for medical treatments are most at risk.
Check for NDC 73198-0018-10 and lots D41219 (BUD 4/19/2022) or I24C13 (BUD 9/13/2022). These vials are prescription-only and sold by Olympia Pharmacy in Orlando, Florida.
Look for NDC 73198-0018-10 and lots D41219 or I24C13 on the vial label.
The vials were produced before October 2021 and had uninvestigated monitoring issues, which could lead to unsafe drug concentrations.
The official recall notice does not specify a remedy or action for affected vials.
Yes, check for lots D41219 (BUD 4/19/2022) or I24C13 (BUD 9/13/2022).
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0798-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0798-2022 from Olympia Pharmacy. 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.
