Talon Compounding Pharmacy recalls specific TEST CYPIONATE 200MG/ANASTROZOLE 0.5MG/DUTASTERIDE 1MG/ML #2 injectable products with lot numbers T1008252021:29 and T1006042021:51 due to lack of sterility assurance. Consumers should contact the pharmacy for details.
Lack of assurance of sterility
Talon Compounding Pharmacy is recalling certain TEST CYPIONATE injectable products because they may not be sterile. This could lead to infections if used improperly. Affected products have specific lot numbers and were sold in San Antonio, Texas.
The products lack assurance of sterility, meaning they might contain harmful bacteria or other contaminants. If injected, this could cause serious infections or other health issues. The hazard is not described in detail about how it occurs or the specific risks.
People who have received the recalled TEST CYPIONATE injectable products with lot numbers T1008252021:29 or T1006042021:51 from Talon Compounding Pharmacy in San Antonio, Texas are affected. Patients using these products for medical treatment are at risk.
Check the product label for lot numbers T1008252021:29 or T1006042021:51. The products were sold by Talon Compounding Pharmacy in San Antonio, Texas.
Look for lot numbers T1008252021:29 or T1006042021:51 on the injectable product.
TEST CYPIONATE 200MG/ANASTROZOLE 0.5MG/DUTASTERIDE 1MG/ML #2 injectable products with lot numbers T1008252021:29 and T1006042021:51.
Talon Compounding Pharmacy in San Antonio, Texas.
Check the product label for lot numbers T1008252021:29 or T1006042021:51.
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-0154-2022 — Talon Compounding Pharmacy Talon Compounding Pharmacy Hello, I own a Talon Compounding Pharmacy that is covered by recall D-0154-2022 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.
