Olympia Pharmacy recalls Formula F9 vials due to lack of sterility assurance. This medication is for prescription use only and may pose infection risks if used improperly.
Lack of assurance of sterility.
Olympia Pharmacy is recalling Formula F9 vials that contain papaverine, phentolamine, PGE, and atropine. The vials lack assurance of sterility, which could lead to infections if used.
The vials lack assurance of sterility, meaning they might not be free from harmful bacteria. If the vial is contaminated, it could cause infections when injected into the body.
Prescription patients who received Formula F9 vials from Olympia Pharmacy. Those with compromised immune systems are at higher risk of infection.
Check for the product name 'Formula F9 Papaverine 0.9 mg/mL Phentolamine 0.1 mg/mL PGE 20 mcg/mL Atropine 0.01 mg/mL, Multi-Dose 10 mL vial'. The NDC code is 73198-0004-10 and lot number B24G02-22.
Look for the NDC code 73198-0004-10 and lot number B24G02-22 on the vial label.
The recall states there is a lack of assurance of sterility, so it is not safe to use. The vials may be contaminated and could cause infections.
The recall does not specify a remedy, so contact Olympia Pharmacy directly for guidance.
Check for the NDC code 73198-0004-10 and lot number B24G02-22 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-0929-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0929-2022 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.
