Olympia Pharmacy recalls SB-4 vials (Papaverine, Phentolamine, Alprostadil) due to improper investigation of environmental monitoring issues before October 2021. Affected vials have specific lot numbers and expiration dates.
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 SB-4 multi-dose vials that contain Papaverine, Phentolamine, and Alprostadil. The recall is due to CGMP deviations where environmental and personnel monitoring issues were not properly investigated before October 2021.
The recall is for CGMP deviations where environmental and personnel monitoring issues were not properly investigated before October 2021. This could mean the vials may not be safe for medical use due to improper quality control.
Prescription patients who received the SB-4 vials with lot numbers E41C18, E41D18, G42D20, or G42B20 from Olympia Pharmacy in Orlando, Florida. Healthcare providers using these vials for medical treatments are most at risk.
Check for vials labeled SB-4 with specific lot numbers: E41C18, E41D18, G42D20, or G42B20. These vials were sold by Olympia Pharmacy in Orlando, Florida with expiration dates up to July 2022.
Look for lot numbers E41C18, E41D18, G42D20, or G42B20 on the vial label.
The recall is due to CGMP deviations where environmental and personnel monitoring issues were not properly investigated before October 2021.
Check the lot number on the vial. If it matches E41C18, E41D18, G42D20, or G42B20, contact Olympia Pharmacy for instructions.
The official notice does not specify safety risks, so the recall is based on potential quality control issues.
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0806-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0806-2022 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.
