Talon Compounding Pharmacy recalls TRI-MIX PAPAVERINE 30/PHENTOLAMINE 0.5/PGE-1 30 INJ injectables due to lack of sterility assurance. This medication is for prescription use only and was manufactured in San Antonio, Texas.
Lack of assurance of sterility
Talon Compounding Pharmacy is recalling a specific prescription medication mix due to a lack of sterility assurance. This means the product could be contaminated, posing a risk of infection if used.
The medication lacks proper sterility assurance, which means it could be contaminated with bacteria or other harmful substances. If injected, this could lead to serious infections or other health complications.
Prescription patients who received this specific medication from Talon Compounding Pharmacy in San Antonio, Texas. Those with medical conditions requiring this medication are most at risk.
Check for the product name 'TRI-MIX PAPAVERINE 30/PHENTOLAMINE 0.5/PGE-1 30 INJ' on the label. The lot number 06252021:22 and batch date 10/23/2021 are specific to this recall.
Look for the product name and lot number 06252021:22 on the label to confirm if it is recalled.
The recall indicates a lack of sterility assurance, so it is not safe to use. The product may be contaminated and could cause infection if injected.
Check the product label for the lot number 06252021:22. If it matches, contact Talon Compounding Pharmacy for instructions.
The recall record does not specify a replacement process. Contact Talon Compounding Pharmacy directly for assistance.
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-0201-2022 — Talon Compounding Pharmacy Talon Compounding Pharmacy Hello, I own a Talon Compounding Pharmacy that is covered by recall D-0201-2022 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.
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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.
