Olympia Pharmacy recalls Atropine Sulfate 50 mg/ml injections due to potential contamination risks from quality control issues. Affected units were compounded in Orlando, FL with expiration 9/11/13.
Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
Olympia Pharmacy recalled Atropine Sulfate 50 mg/ml injections because FDA inspections found quality control issues that could lead to contamination. This affects patients who received these injections, as contaminated products could cause serious health risks.
The FDA found quality control problems during the compounding process, which could result in contaminated injections. Contaminated products might cause infections or other health issues if used.
Patients who received the recalled Atropine Sulfate injections compounded by Olympia Pharmacy in Orlando, FL. Those with medical conditions requiring injections are at higher risk.
Check for the product name 'Atropine Sulfate 50 mg/ml Injection' compounded by Olympia Pharmacy in Orlando, FL. The expiration date is 9/11/13.
Look for the product name and expiration date on the label to confirm if it matches the recalled items.
The FDA has identified quality control issues that could lead to contamination, so it is not safe to use.
Check the product label for 'Atropine Sulfate 50 mg/ml Injection' compounded by Olympia Pharmacy in Orlando, FL with expiration 9/11/13.
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-702-2013 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-702-2013 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.
