Talon Compounding Pharmacy recalls specific TRI-MIX injectable medication due to lack of sterility assurance. This risk could lead to infections if used improperly. Affected patients should contact their healthcare provider for guidance.
Lack of assurance of sterility
Talon Compounding Pharmacy is recalling a specific injectable medication product called TRI-MIX PAPAVERINE 15/PHENTOLAMINE 1/PGE-1 10 INJ due to a lack of sterility assurance. This could lead to infections if the medication is used without proper sterilization.
The medication lacks proper sterility assurance, which means it could be contaminated with bacteria or other harmful substances. If injected without proper sterilization, this could lead to serious infections or other health complications.
Patients prescribed this medication by a healthcare provider in the United States. Those with specific medical conditions requiring this medication are most at risk.
Check for the product name 'TRI-MIX PAPAVERINE 15/PHENTOLAMINE 1/PGE-1 10 INJ' and the lot number '09082021:40' on the label. This medication was sold by Talon Compounding Pharmacy in San Antonio, Texas.
Patients should contact their healthcare provider for guidance on whether they have the recalled medication and what to do next.
The recall indicates a lack of sterility assurance, so it is not safe to use without proper medical guidance.
Contact your healthcare provider for specific instructions on how to handle the recalled medication.
Look for the product name 'TRI-MIX PAPAVERINE 15/PHENTOLAMINE 1/PGE-1 10 INJ' and the lot number '09082021:40' on the label.
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-0188-2022 — Talon Compounding Pharmacy Talon Compounding Pharmacy Hello, I own a Talon Compounding Pharmacy that is covered by recall D-0188-2022 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.
