Olympia Pharmacy recalls Tripelennamine 2:000 mg/ml injections compounded in Orlando, FL due to potential sterility issues. Affected batches expire 8/20/2013 and 12/31/2013. No remedy specified in recall notice.
Lack of Assurance of Sterility: FDA inspection findings resulted in concerns regarding quality control processes
Olympia Pharmacy recalled specific batches of Tripelennamine 20 mg/ml injections compounded in Orlando, Florida. The recall is due to FDA concerns about sterility quality control processes, which could pose a risk of infection if used.
The FDA found issues with Olympia Pharmacy's quality control processes during inspections. This lack of sterility assurance could lead to infections if the injections are used, as they are compounded medications.
People who received Tripelennamine 20 mg/ml injections compounded by Olympia Pharmacy in Orlando, Florida between the expiration dates listed. Patients using these injections for medical treatment are at risk of infection.
Check for the batch numbers B5620 (expiring 8/20/2013) or A0322 (expiring 12/31/2013) on the injection vials. These were compounded by Olympia Pharmacy in Orlando, Florida.
Look for batch numbers B5620 (expiring 8/20/2013) or A0322 (expiring 12/31/2013) on the injection vials.
The FDA found concerns about Olympia Pharmacy's quality control processes during inspections, which could lead to sterility issues in the compounded injections.
The recall notice does not specify a remedy, so check the batch numbers and contact Olympia Pharmacy for guidance.
The recall indicates potential sterility issues, which could cause infections if the injections are used. However, the exact risk level is not specified in the notice.
We’ve drafted a message you can send Olympia Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-788-2013 — Olympia Pharmacy Olympia Pharmacy Hello, I own a Olympia Pharmacy that is covered by recall D-788-2013 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.
