Olympia Pharmacy recalls testosterone cypionate 200 mg/mL in grapeseed oil vials due to improper investigation of environmental and personnel monitoring out-of-action limit excursions before October 2021.
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 testosterone cypionate 200 mg/mL in grapeseed oil vials because of CGMP deviations. This means the product may not have been properly checked for safety before October 2021, which could affect quality.
The product was made before October 2021 without proper investigation of environmental and personnel monitoring issues. This could mean the product wasn't checked for safety as required by regulations, potentially affecting quality.
People who have the recalled testosterone vials (10 mL or 5 mL multi-dose) from Olympia Pharmacy in Orlando, FL. Those using the product for medical purposes are most at risk.
Check for vials labeled 'Testosterone Cypionate 200 mg/mL (in Grapeseed Oil)' with NDC numbers 73198-0054-10 (10 mL) or 73198-0054-05 (5 mL). The product was sold with specific batch numbers and expiration dates.
Look for the NDC numbers 73198-0054-10 or 73198-0054-05 on the vial label.
The product was made before October 2021 without proper investigation of environmental and personnel monitoring issues, which could affect quality.
The recall record does not specify a remedy, so no action is required beyond checking if you have the product.
The recall record does not state that the product is unsafe; it indicates potential quality issues due to CGMP deviations.
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0823-2022 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-0823-2022 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.
