Olympia Pharmacy recalls QM-4 Papaverine vials due to lack of sterility assurance. This multi-dose medication may cause infections if used improperly.
Lack of assurance of sterility.
Olympia Pharmacy is recalling QM-4 Papaverine vials that could be contaminated, posing infection risks. This recall affects patients using the medication as prescribed.
The vials lack proper sterility assurance, which means they could become contaminated during storage or use. This contamination risk may lead to infections if the medication is injected.
Patients prescribed QM-4 Papaverine vials by a doctor. Those using the medication for medical purposes are most at risk.
Check for the QM-4 Papaverine 30 mg/mL Phentolamine 3 mg/mL Alprostadil 300 mcg/mL Atropine 0.2 mg/mL, Multi-Dose 10 mL vial with NDC 73198-0020-10. The lot number L24F08 was manufactured until December 8, 2022.
Verify the product name, NDC number, and lot number to confirm if it's recalled.
The recall states there is a lack of sterility assurance, so it may be contaminated. Do not use the vial if it's part of the recalled batch.
Look for the NDC 73198-0020-10 and lot number L24F08 on the vial label. The vial was manufactured until December 8, 2022.
The recall does not specify a remedy, so contact your doctor or pharmacist 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-0897-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0897-2022 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.
