Olympia Pharmacy recalls Alprostadil 80 mcg/mL 10ml vials (NDC 73198-0029-10) manufactured before Oct 2021 due to unaddressed quality control deviations. No specific action steps listed in recall notice.
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 Alprostadil 80 mcg/mL 10ml multi-dose vials (NDC 73198-0029-10) that were made before October 2021. These vials were produced under quality control issues that could affect safety.
The recall is due to quality control issues where environmental and personnel monitoring failures were not properly investigated before October 2021. This could lead to unsafe medication if the vial was not properly monitored during production.
Prescription patients who received this specific Alprostadil vial from Olympia Pharmacy before October 2021. Patients using this medication for erectile dysfunction are most at risk.
Check for the product name 'Alprostadil 80 mcg/mL 10ml Multi-Dose vial', NDC 73198-0029-10, and lot number F48102 manufactured before October 2021.
Verify the product name, NDC number, and lot number to confirm if it matches the recalled items.
The recall notice states there were quality control issues, but does not specify if the product is safe to use. No specific action steps are listed in the recall notice.
The recall notice does not provide specific action steps for affected customers. Check with Olympia Pharmacy for further instructions.
Look for the product name 'Alprostadil 80 mcg/mL 10ml Multi-Dose vial', NDC 73198-0029-10, and lot number F48102 manufactured before October 2021.
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0818-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0818-2022 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.
