Olymp: Glutathione 200 mg/ml injection compounded by Olympia Pharmacy in Orlando, FL has been recalled due to lack of sterility assurance. FDA inspection found quality control issues.
Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
Olympia Pharmacy recalled Glutathione 200 mg/ml injections compounded in Orlando, FL because FDA inspections found quality control problems that could lead to contamination. This affects patients using the injection for medical treatment.
The FDA found that Olympia Pharmacy's quality control processes were inadequate, which could result in the injection not being sterile. Contaminated injections can cause serious infections or other health issues if used.
Patients who received the Glutathione 200 mg/ml injection compounded by Olympia Pharmacy in Orlando, FL between the time of compounding and expiration date of September 11, 2013. Those with medical conditions requiring injections are at higher risk.
Check for the product name 'Glutathione 200 mg/ml Injection' compounded by Olympia Pharmacy in Orlando, FL. The expiration date on the label is September 11, 2013 (C5110).
Look for the expiration date 'C5110 Exp 9/11/13' on the injection label.
The FDA has identified quality control issues that could lead to contamination, so the product is not safe to use.
Check for the product name 'Glutathione 200 mg/ml Injection' compounded by Olympia Pharmacy in Orlando, FL with expiration date September 11, 2013.
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-736-2013 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-736-2013 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.
