Olymp: 25 mg/ml Acepromazine injection compounded by Olympia Pharmacy in Orlando, FL is recalled due to potential contamination risks from quality control issues. No remedy specified.
Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
Olympia Pharmacy recalled 25 mg/ml Acepromazine injections compounded in Orlando, FL because FDA inspections found quality control issues that could lead to contamination. This affects veterinary use and requires immediate attention due to potential health risks.
FDA inspections found quality control problems during the compounding process that could result in contamination. This means the injections might not be sterile, posing a risk of infection or other health issues when used in animals.
Veterinarians and pet owners using Acepromazine injections for animals. Those who received the specific batch (B0112 exp 08/31/13) in Orlando, FL are most at risk.
Check for the batch number B0112 with expiration date 08/31/13 on the label. The product was compounded by Olympia Pharmacy in Orlando, Florida.
Look for the batch number B0112 and expiration date 08/31/13 on the Acepromazine injection label.
The FDA found quality control issues during compounding, so the product may not be sterile. It is not safe to use as recalled.
The recall record does not specify a remedy, so contact Olympia Pharmacy directly for guidance.
Check for the batch number B0112 with expiration date 08/31/13 on the label. The product was compounded by Olympia Pharmacy in Orlando, Florida.
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-693-2013 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-693-2013 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.
