Olympia Pharmacy recalls Vitamin D3 (50,000 IU/mL) multi-dose vials due to lack of sterility assurance. This affects specific lots and expiration dates. Consumers should check their product details and contact the pharmacy for guidance.
Lack of assurance of sterility.
Olympia Pharmacy is recalling Vitamin D3 (50,000 IU/mL) multi-dose vials because they may not be sterile. This could lead to infections if used improperly. The recall affects specific lots with expiration dates from June 2022.
The vials lack assurance of sterility, meaning they might contain harmful bacteria or other contaminants. If the vial is used without proper sterilization, it could cause infections, especially in medical settings where sterility is critical.
People who have the specific Vitamin D3 vials with lot numbers L24009 or L24028 and expiration dates up to June 28, 2022 are affected. Those using prescription vitamin D3 for medical reasons are most at risk.
Check for the product name 'Vitamin D3 (50,000 IU/mL) Multi-Dose 30 mL vial, Rx Only' and lot numbers L24009 or L24028 with expiration dates up to June 28, 2022.
Look for the lot numbers L24009 or L24028 and expiration dates up to June 28, 2022 on the vial.
The recall states there is a lack of sterility assurance, so it may not be safe. The manufacturer recommends checking the product details and contacting them for guidance.
The recall does not specify a remedy, so contact Olympia Pharmacy directly for instructions on what to do with the product.
Check for lot numbers L24009 or L24028 with expiration dates up to June 28, 2022 on the vial.
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0915-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0915-2022 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.
