Olympia Pharmacy recalls SB-5 vials (Papaverine 30 mg/mL, Phentolamine 3 mg/mL, PGE 50 mcg/mL) due to improper investigation of environmental and personnel monitoring deviations before October 2021. This may affect safety in medical use.
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-5 multi-dose vials that were made before October 2021. The vials may have safety issues because the company didn't properly investigate monitoring problems that could affect quality.
The vials were made before October 2021 and had uninvestigated monitoring deviations. This could mean the vials don't meet safety standards for medical use, but the risk is low for most patients.
People with prescriptions for SB-5 vials from Olympia Pharmacy. Those using the vials for medical purposes are most at risk.
Check for SB-5 vials labeled with NDC 73198-0024-10. Look for lot numbers E48B18, E48D18, H24D31, or E48C18 with expiration dates up to May 2022 or August 2022.
Look for NDC 73198-0024-10 and lot numbers E48B18, E48D18, H24D31, or E48C18.
The vials were made before October 2021 and had uninvestigated monitoring deviations, which could affect safety standards for medical use.
Check for NDC 73198-0024-10 and lot numbers E48B18, E48D18, H24D31, or E48C18.
The recall record does not specify a remedy, so contact Olympia Pharmacy directly 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-0807-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0807-2022 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.
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.
