Olympia Pharmacy recalls specific alprostadil vials (NDC 73198-0028-10) due to improper investigation of quality control deviations. Affected vials have batch numbers I24028, F47C30, and F47B30 with expiration dates up to September 2022.
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 vials that were manufactured before October 2021 because quality control issues were not properly addressed. This could lead to unsafe medication if used without the recall fix.
The vials were produced before October 2021 and had quality control issues that weren't properly investigated. This could mean the medication might not be safe for use, potentially causing harm to patients.
Prescription patients who received the specific alprostadil vials with batch numbers I24028, F47C30, or F47B30. Patients using these vials for medical treatment are most at risk.
Check the vial label for the product name 'Alprostadil 40 mcg/mL, 10ml Multi-Dose vial' and the batch numbers I24028, F47C30, or F47B30. The expiration dates are up to September 2022.
Look for the batch numbers I24028, F47C30, or F47B30 on the vial label.
The product is Alprostadil 40 mcg/mL, 10ml Multi-Dose vial (NDC 73198-0028-10) prescribed by a doctor.
Check the vial label for batch numbers I24028, F47C30, or F47B30 with expiration dates up to September 2022.
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-0817-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0817-2022 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.
