Olympia Pharmacy recalls Sodium Selenite 200 mg/mL vials due to lack of sterility assurance. This affects prescription-only multi-dose vials with specific lot numbers and expiration dates.
Lack of assurance of sterility.
Olympia Pharmacy is recalling prescription sodium selenite vials because they may not be sterile. Using these vials could lead to infections if the medication is contaminated.
The vials lack proper sterility assurance, meaning they could become contaminated during storage or use. This contamination risk could lead to infections, especially for individuals with weakened immune systems.
Prescription patients who received this specific sodium selenite vial from Olympia Pharmacy. Those with compromised immune systems are at higher risk of infection.
Check for the product name 'Sodium Selenite 200 mg/mL, Multi-Dose 30 mL vial, Rx Only' from Olympia Pharmacy. Look for lot numbers L24014 (BUD: 6/14/2022) or L24024-22 (BUD: 8/24/2022).
Identify the lot number and expiration date on the vial label to confirm if it's part of the recall.
The recall states there is a lack of sterility assurance, so these vials may be contaminated. Do not use them.
The recall does not specify a remedy, so contact Olympia Pharmacy directly for guidance.
Look for lot numbers L24014 (BUD: 6/14/2022) or L24024-22 (BUD: 8/24/2022) 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-0905-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0905-2022 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.
