Talon Compounding Pharmacy recalls TRI-MIX PAPAVERINE 30/PHENTOLAMINE 2/PGE-1 50 INJ injectables due to lack of sterility assurance. This medication is prescription-only and may pose infection risks if used.
Lack of assurance of sterility
Talon Compounding Pharmacy is recalling a specific prescription injectable medication because it lacks sterility assurance. This could lead to infections if the medication is used without proper sterility.
The medication was produced without proper sterility assurance, meaning it could contain harmful bacteria or other contaminants. This poses a risk of infection if the medication is administered into the body.
Prescription patients who received this specific injectable medication from Talon Compounding Pharmacy in San Antonio, Texas. Those with the lot numbers 07082021:16 or 08172021:26 are most at risk.
Check the product label for the lot numbers 07082021:16 or 08172021:26. The medication is prescription-only and sold by Talon Compounding Pharmacy in San Antonio, Texas.
Look for the lot numbers 07082021:16 or 08172021:26 on the medication label.
The recall states there is a lack of sterility assurance, which could lead to infections if used. It is not safe to use without contacting the manufacturer.
Check the product label for lot numbers 07082021:16 or 08172021:26. This medication is prescription-only and sold by Talon Compounding Pharmacy in San Antonio, Texas.
The recall does not specify a remedy, so contact Talon Compounding Pharmacy 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-0214-2022 — Talon Compounding Pharmacy Talon Compounding Pharmacy Hello, I own a Talon Compounding Pharmacy that is covered by recall D-0214-2022 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.
