Talon Compounding Pharmacy recalls specific injectable medication products due to lack of sterility assurance. This affects certain lots manufactured between November 2021 and March 2022. Consumers should contact the pharmacy for details.
Lack of assurance of sterility
Talon Compounding Pharmacy has recalled specific injectable medication products because they lack sterility assurance. This means the products could be contaminated and unsafe for use, especially since they are prescription-only medications.
The medication products were manufactured without proper sterility assurance, which means they could be contaminated with harmful bacteria. This poses a risk of infection or other health issues if used improperly.
Prescription patients who received the recalled medication from Talon Compounding Pharmacy. Those with the specific lot numbers listed in the recall notice are most at risk.
Check the product label for the specific lot numbers: T1005172021:27 (expires 11/13/2021), T1007222021:42 (expires 01/18/2022), or T1009162021:45 (expires 03/15/2022).
Look for the lot numbers listed in the recall: T1005172021:27, T1007222021:42, or T1009162021:45.
The medication lacks sterility assurance, which means it could be contaminated with harmful bacteria.
Check the product label for the specific lot numbers: T1005172021:27 (expires 11/13/2021), T1007222021:42 (expires 01/18/2022), or T1009162021:45 (expires 03/15/2022).
Contact Talon Compounding Pharmacy for instructions on what to do with the medication.
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-0161-2022 — Talon Compounding Pharmacy Talon Compounding Pharmacy Hello, I own a Talon Compounding Pharmacy that is covered by recall D-0161-2022 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.
