Talon Compounding Pharmacy recalls specific lots of TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1/PGE-1 12 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 specific lots of TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1/PGE-1 12 INJ injectables because they lack sterility assurance. This means the medication could cause infections if used improperly.
The medication lacks sterility assurance, meaning it could be contaminated with bacteria or other pathogens. This poses a risk of infection if the injectable is used, especially since it's a prescription medication administered directly into the body.
Prescription patients who received the recalled lots of TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1/PGE-1 12 INJ injectables from Talon Compounding Pharmacy. Those with the specific lot numbers listed in the recall are most at risk.
Check the product label for the lot numbers: 07092021:34, 08302021:33, 08162021:08, 08262021:31, or 09152021:63. The medication is sold by Talon Compounding Pharmacy in San Antonio, Texas.
Look for the lot numbers listed in the recall: 07092021:34, 08302021:33, 08162021:08, 08262021:31, or 09152021:63.
The recall states there is a lack of sterility assurance, which means it could cause infections if used. Do not use the recalled lots.
The recall does not specify a remedy, so contact Talon Compounding Pharmacy for guidance on safe disposal or alternatives.
Check the product label for the lot numbers: 07092021:34, 08302021:33, 08162021:08, 08262021:31, or 09152021:63.
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-0204-2022 — Talon Compounding Pharmacy Talon Compounding Pharmacy Hello, I own a Talon Compounding Pharmacy that is covered by recall D-0204-2022 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.
