Talon Compounding Pharmacy recalls specific TRI-MIX injectable products for lack of sterility assurance. This affects certain lots manufactured in San Antonio, Texas. Consumers should contact the pharmacy for details.
Lack of assurance of sterility
Talon Compounding Pharmacy is recalling specific TRI-MIX injectable products because they may not be sterile. This could lead to infections if used improperly. The recall affects patients prescribed these medications.
The product lacks assurance of sterility, meaning it might contain harmful bacteria or other contaminants. If injected, this could cause serious infections or other health issues. However, the exact risk level is not clearly described in the recall notice.
Patients prescribed TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1.5/PGE-1 50 INJ injections by a doctor. Those who have received the recalled lot numbers from Talon Compounding Pharmacy in San Antonio, Texas are most at risk.
Check the product label for the lot numbers 07162021:14 (BUD: 11/30/2021) or 09142021:63 (BUD: 02/08/2022). The product is sold by Talon Compounding Pharmacy in San Antonio, Texas.
Look for lot numbers 07162021:14 or 09142021:63 on the product label.
The recall states there is a lack of assurance of sterility, which could pose a health risk. The official notice does not specify if the product is safe to use.
The recall does not provide specific action steps for consumers. Contact Talon Compounding Pharmacy for further instructions.
Check the product label for lot numbers 07162021:14 (BUD: 11/30/2021) or 09142021:63 (BUD: 02/08/2022).
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-0203-2022 — Talon Compounding Pharmacy Talon Compounding Pharmacy Hello, I own a Talon Compounding Pharmacy that is covered by recall D-0203-2022 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.
