Olympia Pharmacy recalls specific multi-dose vials of F2 Papaverine due to lack of sterility assurance. This could lead to infections if used improperly. Affected vials have NDC 73198-0002-10 and lot numbers A24F19-22.
Lack of assurance of sterility.
Olympia Pharmacy is recalling multi-dose vials of F2 Papaverine that may not be sterile. Using these vials could lead to infections if they are not properly handled or stored.
The vials lack assurance of sterility, meaning they might contain harmful bacteria. If the vials are used without proper cleaning or storage, this could lead to infections.
Patients prescribed this medication by a doctor are likely affected. Those using the vials without proper sterility checks are at higher risk.
Check for the NDC number 73198-0002-10 and lot number A24F19-22 on the vial label. These vials were sold with a batch expiration date of January 19, 2023.
Look for the NDC number 73198-0002-10 and lot number A24F19-22 on the vial label.
The recall states there is a lack of assurance of sterility, so it is not safe to use without proper checks.
The recall does not specify a remedy, so contact your doctor for guidance on whether to stop using it.
Check for the NDC number 73198-0002-10 and lot number A24F19-22 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-0928-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0928-2022 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.
