Talon Compounding Pharmacy recalls specific TRI-MIX injectable medication due to lack of sterility assurance. This product is for prescription use only and may pose infection risks if used.
Lack of assurance of sterility
Talon Compounding Pharmacy is recalling a specific injectable medication product (TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1/PGE-1 25 INJ 106) because it lacks sterility assurance. This could lead to infection risks if the medication is used without proper sterility.
The medication lacks assurance of sterility, meaning it may contain harmful bacteria or other contaminants that could cause infections when injected into the body. This is a serious risk for patients who require this medication for medical treatment.
Prescription patients who received this specific injectable 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 1/PGE-1 25 INJ 106' on the label. The lot number 07232021:18 and expiration date 11/30/2021 are specific identifiers for this recall.
Look for the product name 'TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1/PGE-1 25 INJ 106' and lot number 07232021:18 on the label.
The official recall states there is a lack of assurance of sterility, so this product is not safe to use without proper testing.
The recall does not specify a remedy, so contact Talon Compounding Pharmacy directly for guidance.
Check the product label for the name 'TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1/PGE-1 25 INJ 106' and lot number 07232021:18.
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-0207-2022 — Talon Compounding Pharmacy Talon Compounding Pharmacy Hello, I own a Talon Compounding Pharmacy that is covered by recall D-0207-2022 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.
