Olympia Pharmacy recalls Lidocaine 1%/Epinephrine 1:100,000/mL multi-dose vials due to lack of sterility assurance. This could lead to infections if used improperly.
Lack of assurance of sterility.
Olympia Pharmacy is recalling multi-dose lidocaine and epinephrine vials because they may not be sterile. Using these vials could lead to infections, especially if they are reused.
The vials lack sterility assurance, meaning they could become contaminated during use. This increases the risk of infection, particularly if the vials are reused multiple times.
Patients prescribed this medication by a doctor. Those using the vials for multiple injections are at higher risk of infection.
Check for the product name: Lidocaine 1%/Epinephrine 1:100,000/mL, Multi-Dose 30 mL vial. The manufacturer is Olympia Pharmaceuticals, and the NDC code is 73198-0099-30. The lot number is K41023 with a batch date ending May 23, 2022.
Look for the NDC code 73198-0099-30 and lot number K41023 on the vial label.
The product may not be sterile, so it could cause infections if reused. Do not use the vials without checking the recall.
Check for the NDC code 73198-0099-30 and lot number K41023 on the vial label.
The recall 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-0931-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0931-2022 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.
