Olympia Pharmacy recalls multi-dose vials of Papaverine, Phentolamine, and Alprostadil due to improper investigation of environmental and personnel monitoring deviations before October 2021. This may affect prescription drug safety.
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 multi-dose vials of Papaverine, Phentolamine, and Alprostadil that were manufactured before October 2021. These vials could have quality control issues that might affect drug safety if used improperly.
The recall is due to improper investigation of environmental and personnel monitoring deviations before October 2021. This means the vials might not meet quality standards, potentially affecting drug safety.
Prescription drug users who received these specific vials from Olympia Pharmacy before October 2021. Patients using these medications for medical treatments are most at risk.
Check for vials labeled 'RE-2, Papaverine 30 mg/mL . Phentolamine 3 mg/mL . Alprostadil 300 mcg/mL, Multi-Dose 10 mL' from Olympia Pharmacy. Look for lot numbers E42G11, H41003, or H41B03 with expiration dates up to May 2022 or August 2022.
Identify the vial by checking for the product name and lot numbers listed in the recall notice.
The recall is due to improper investigation of environmental and personnel monitoring deviations before October 2021, which could affect quality standards.
The recall notice does not specify a remedy, so check with Olympia Pharmacy for guidance on next steps.
Look for vials labeled 'RE-2, Papaverine 30 mg/mL . Phentolamine 3 mg/mL . Alprostadil 300 mcg/mL, Multi-Dose 10 mL' with lot numbers E42G11, H41003, or H41B03.
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0814-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0814-2022 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.
