Talon Compounding Pharmacy recalls MIC B12 25/50/50/0.5MG/ML L-Carnitine 250MG/ML Injectable (Rx only) due to lack of sterility assurance. Affected units were manufactured on 10/25/2021 with lot number 07272021:62.
Lack of assurance of sterility
Talon Compounding Pharmacy has recalled a specific injectable medication product due to a lack of sterility assurance. This means the product could be contaminated with bacteria, posing a risk of infection if used.
The product lacks assurance of sterility, meaning it may contain bacteria or other contaminants. If injected, this could lead to serious infections or other health complications.
People who have received the MIC B12 25/50/50/0.5MG/ML L-Carnitine 250MG/ML Injectable from Talon Compounding Pharmacy in San Antonio, Texas. Patients using this medication for medical purposes are at risk of infection.
Check for the product name: MIC B12 25/50/50/0.5MG/ML L-Carnitine 250MG/ML Injectable (Rx only). Look for the lot number 07272021:62 and the batch date of 10/25/2021 on the label.
Look for the lot number 07272021:62 and batch date of 10/25/2021 on the product label.
The product has been recalled due to a lack of sterility assurance, so it is not safe to use. The manufacturer advises checking the label for the specific lot number and batch date.
The recall record does not specify a remedy, so the official notice does not provide instructions on what to do with the product.
Check the product label for the lot number 07272021:62 and batch date of 10/25/2021.
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-0132-2022 — Talon Compounding Pharmacy Talon Compounding Pharmacy Hello, I own a Talon Compounding Pharmacy that is covered by recall D-0132-2022 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.
