Olympia Pharmacy recalls Alprostadil 150 mcg/mL 10ml vials (NDC 73198-0030-10) due to improper investigation of environmental and personnel monitoring deviations before October 2021. This affects prescription-only medication.
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 150 mcg/mL 10ml multi-dose vials (NDC 73198-0030-10) because quality control issues occurred before October 2021. This recall affects patients prescribed this medication for specific medical conditions.
The recall is due to environmental and personnel monitoring deviations that weren't properly investigated before October 2021. This could potentially lead to medication quality issues, but the exact risk to patients isn't specified in the recall notice.
Patients prescribed Alprostadil 150 mcg/mL 10ml vials by a doctor are affected. Those with the specific NDC number and lot code G24C19 are most at risk.
Check for the NDC number 73198-0030-10 and lot code G24C19 on the vial label. The product was sold by Olympia Pharmacy in Orlando, Florida, with a batch expiration date of July 19, 2022.
Look for NDC 73198-0030-10 and lot code G24C19 on the vial label.
The recall notice states there were quality control issues before October 2021, but does not specify if the medication is safe to use. Patients should contact their doctor for guidance.
The recall notice does not mention a replacement or remedy process. Patients should contact their doctor or Olympia Pharmacy directly.
The product has a batch expiration date of July 19, 2022, as indicated on the vial label.
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0819-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0819-2022 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.
