Olympia Pharmacy recalls specific vials of Papaverine, Phentolamine, and Alprostadil due to improper investigation of environmental and personnel monitoring deviations before October 2021. This may affect patients using these medications.
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 certain vials of Papaverine, Phentolamine, and Alprostadil that were manufactured before October 2021. These vials may have had improper investigation of environmental and personnel monitoring issues, which could lead to medication safety concerns.
The recall is due to CGMP deviations where environmental and personnel monitoring out-of-action limits were not properly investigated before October 2021. This could mean the medication may not be safe for use as intended.
Patients using the recalled vials for medical treatment are affected. Those with specific prescription orders for these medications are most at risk.
Check for vials labeled 'RE-1, Papaverine 30 mg/mL . Phentolamine 3 mg/mL . Alprostadil 200 mcg/mL' with NDC numbers 73198-0015-10 or 73198-0015-03. The vials were sold with specific lot numbers and expiration dates.
Identify the NDC numbers and lot numbers on the vial to confirm if it is part of the recall.
The recall is due to CGMP deviations where environmental and personnel monitoring out-of-action limits were not properly investigated before October 2021.
The official notice does not specify a remedy or action for the recalled vials.
Yes, the recall includes vials with lot numbers E47B18 (BUD: 5/18/2022) and E47C18 (BUD: 5/18/2022) or H24G31 (BUD: 8/31/2022).
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0813-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0813-2022 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.
