Talon Compounding Pharmacy recalls ALPROSTADIL 22MCG/ML injectable (Rx only) due to lack of sterility assurance. This may pose infection risks. Check your product lot number for affected items.
Lack of assurance of sterility
Talon Compounding Pharmacy is recalling ALPROSTADIL 22MCG/ML injectable (Rx only) because it lacks sterility assurance. This could lead to infections if used improperly. Affected items have a specific lot number and were sold in San Antonio, Texas.
The product lacks sterility assurance, meaning it may not be free from harmful microorganisms. If injected, this could cause infections or other health issues. The lack of sterility is a critical safety concern for medical use.
People with prescriptions for ALPROSTADIL 22MCG/ML injectable from Talon Compounding Pharmacy in San Antonio, Texas. Those using the product without proper sterility assurance are at risk of infection.
Check for the lot number 06082021:61 on the product label. The product was sold by Talon Compounding Pharmacy in San Antonio, Texas with a batch date of 10/06/2021.
Look for the lot number 06082021:61 on the ALPROSTADIL 22MCG/ML injectable label.
The recall states there is a lack of sterility assurance, which could pose infection risks. The product is not safe to use as recalled.
The recall does not specify a remedy, so check the product label for the lot number and contact Talon Compounding Pharmacy for further instructions.
Check for the lot number 06082021:61 on the product label. The product was sold by Talon Compounding Pharmacy in San Antonio, Texas with a batch date of 10/06/2021.
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-0100-2022 — Talon Compounding Pharmacy Talon Compounding Pharmacy Hello, I own a Talon Compounding Pharmacy that is covered by recall D-0100-2022 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.
