Olympia Pharmacy recalls specific batches of Phentol: 20 mg/ml injection compounded in Orlando, FL due to quality control concerns affecting sterility. No remedy stated in official notice.
Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
Olympia Pharmacy recalled specific batches of Phentolamine 20 mg/ml injection compounded in Orlando, FL because FDA inspections found quality control issues that could risk contamination. This affects patients using the injection for medical purposes.
The FDA found quality control problems during production that could lead to contamination. This means the injection might not be sterile, which can cause serious infections if used improperly.
Patients who received the recalled batches of Phentolamine 20 mg/ml injection compounded by Olympia Pharmacy in Orlando, FL are at risk. Those using the injection for medical treatments may be affected.
Check the batch numbers on the vial: B31012 (exp 8/31/13), B5102 (exp 8/10/13), C5228 (exp 9/22/13), B5012 (exp 12/31/13), and C5111 (exp 9/11/13). These batches were compounded by Olympia Pharmacy in Orlando, FL.
Look for batch numbers B31012, B5102, C5228, B5012, or C5111 on the vial.
FDA inspections found quality control issues that could lead to contamination, risking non-sterile injections.
The official recall notice does not state a remedy, so contact Olympia Pharmacy directly for guidance.
The recall is due to potential contamination, which could cause infection, but the official notice does not specify the risk level.
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-770-2013 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-770-2013 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.
