Talon Compounding Pharmacy recalls specific lots of TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1/PGE-1 2.5 INJ injectables due to lack of sterility assurance. This medication is for prescription use only.
Lack of assurance of sterility
Talon Compounding Pharmacy has recalled specific lots of TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1/PGE-1 2.5 INJ injectables because they lack sterility assurance. This means the medication could be contaminated, posing a risk of infection if used.
The medication lacks sterility assurance, meaning it could be contaminated with bacteria or other pathogens. If injected, this could lead to serious infections or other health complications.
Prescription patients who received the recalled lots of TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1/PGE-1 2.5 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 specific lot numbers: 07222021:11, 08172021:72, 06282021:84, 07132021:93, or 09102021:43. These lots were manufactured by Talon Compounding Pharmacy in San Antonio, Texas.
Look for the specific lot numbers listed in the recall: 07222021:11, 08172021:72, 06282021:84, 07132021:93, or 09102021:43.
Talon Compounding Pharmacy recalls specific lots of TRI-MIX PAPAVERINE 30/PHENTOLAMINE 1/PGE-1 2.5 INJ injectables due to lack of sterility assurance.
Check the product label for the specific lot numbers: 07222021:11, 08172021:72, 06282021:84, 07132021:93, or 09102021:43.
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-0205-2022 — Talon Compounding Pharmacy Talon Compounding Pharmacy Hello, I own a Talon Compounding Pharmacy that is covered by recall D-0205-2022 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.
