Olympia Pharmacy recalls Sermorelin Acetate multi-dose vials due to improper investigation of environmental and personnel monitoring out-of-action limits before October 2021. Affected lots have specific batch numbers and expiration dates.
CGMP Deviations: prior to October 1, 2021, environmental and personnel monitoring Out of Action Limit (OOAL) excursions were not being properly investigated
Olympia Pharmacy is recalling Sermorelin Acetate multi-dose vials that were manufactured before October 2021. This recall is due to CGMP deviations where monitoring issues were not properly investigated, which could lead to unsafe drug conditions.
The recall is for vials produced before October 2021 that had CGMP deviations. Environmental and personnel monitoring out-of-action limits were not properly investigated, which could lead to unsafe drug conditions.
People who have the recalled Sermorelin Acetate vials with specific batch numbers and expiration dates. Those using the product for medical treatment are most at risk due to potential contamination.
Check for vials labeled 'Sermorelin Acetate, Lyophilized powder for reconstitution, Multi-Dose vials' with specific batch numbers (D41019, D41112, etc.) and expiration dates listed in the recall notice.
Identify the batch number and expiration date on the vial to see if it matches the recalled lots listed in the notice.
The recall is due to CGMP deviations where environmental and personnel monitoring out-of-action limits were not properly investigated before October 2021.
Sermorelin Acetate multi-dose vials with batch numbers D41019, D41112, D47028, F24009, F41001, G48006, G48008, G48012, G48014, G48019, I24009, I41107.
Look for vials with the specific batch numbers and expiration dates listed in the recall notice.
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0797-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0797-2022 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.
