Olympia Pharmacy recalls Sermorelin Acetate Lyophilized powder for reconstitution 9 mg multi-dose vials due to lack of sterility assurance. Affected units have specific NDC and batch numbers.
Lack of assurance of sterility.
Olympia Pharmacy is recalling Sermorelin Acetate Lyophilized powder for reconstitution 9 mg multi-dose vials because they lack sterility assurance. This could lead to infections if the product is used without proper sterilization.
The product lacks sterility assurance, meaning it may not be free from harmful bacteria or contaminants. If the product is used without proper sterilization, it could cause infections or other health issues.
People with prescriptions for Sermorelin Acetate Lyophilized powder from Olympia Pharmacy are affected. Those using the product without proper sterilization are at higher risk.
Check for the NDC number 73198-0059-00 on the vial label. The product was sold with specific batch numbers: L24115 (BUD: 12/15/2022), A24203 (BUD: 01/03/2023), and A24106 (BUD: 01/06/2023).
Look for the NDC number 73198-0059-00 and batch numbers L24115, A24203, or A24106 on the vial.
The recall states there is a lack of sterility assurance, so it may not be safe to use without proper sterilization.
Check the vial label for NDC 73198-0059-00 and batch numbers L24115, A24203, or A24106.
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-0902-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0902-2022 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
