Olympia Pharmacy recalls T-50 vials with CGMP deviations from October 2021. These multi-dose vials may have uninvestigated environmental monitoring issues. Return or contact for remedy.
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 T-50 vials containing Papaverine, Phentolamine, and Alprostadil. The recall is due to CGMP deviations where past monitoring issues weren't properly investigated before October 2021. This could affect medication safety for patients using these prescription vials.
The recall involves CGMP deviations where environmental and personnel monitoring issues were not properly investigated before October 2021. This could mean the vials may have safety risks due to unaddressed monitoring problems.
Patients with prescriptions for T-50 vials from Olympia Pharmacy. Those using the vials for medical treatments are most at risk.
Check for the T-50 vial with Papaverine 8 mg/mL, Phentolamine 0.29 mg/mL, and Alprostadil 2.9 mcg/mL. Look for lot numbers G24F01, G41316, H24B03, or H24C03 with expiration dates up to August 2022.
Identify the vial by checking the product name, lot number, and expiration date on the packaging.
The recall states there were CGMP deviations, but the official notice does not specify if the vial is safe to use.
Check for the T-50 vial with Papaverine 8 mg/mL, Phentolamine 0.29 mg/mL, and Alprostadil 2.9 mcg/mL, and lot numbers G24F01, G41316, H24B03, or H24C03.
The recall record does not specify a remedy, so contact Olympia Pharmacy for guidance.
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0820-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0820-2022 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.
