Talon Compounding Pharmacy recalls specific TRI-MIX injectable medication due to lack of sterility assurance. This risk could lead to infections if used improperly.
Lack of assurance of sterility
Talon Compounding Pharmacy is recalling a specific injectable medication (TRI-MIX PAPAVERINE 17.65/PHENTOLAMINE 0.59/PGE-1 5.9 INJ T 101) because it may not be sterile. Using this product could lead to infections, especially since it's a prescription medication.
The medication may not be sterile, which can lead to infections if injected. This is a serious risk for patients who need this medication for medical treatment.
Prescription patients who received this specific injectable medication from Talon Compounding Pharmacy. Those with medical conditions requiring this medication are at higher risk.
Check for the product name 'TRI-MIX PAPAVERINE 17.65/PHENTOLAMINE 0.59/PGE-1 5.9 INJ T 101' and lot number 07262021:32. This medication was sold by Talon Compounding Pharmacy in San Antonio, Texas.
Look for the lot number 07262021:32 on the medication label to confirm if it's affected.
The recall states there is a lack of assurance of sterility, which means it could cause infections. Do not use this product without confirming it's not recalled.
Check the lot number on the label. If it's 07262021:32, contact Talon Compounding Pharmacy for instructions.
The recall record shows no remedy is specified, so contact the manufacturer directly for guidance.
We’ve drafted a message you can send Talon Compounding Pharmacy to request your refund or repair — edit it as you like.
Subject: Recall D-0190-2022 — Talon Compounding Pharmacy Talon Compounding Pharmacy Hello, I own a Talon Compounding Pharmacy that is covered by recall D-0190-2022 from Talon Compounding 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
