Vital Care Compounder recalls moxefloxacin syrup due to lack of sterility assurance. Products may be contaminated, posing infection risks. Check lot numbers for affected items.
Lack of Assurance of Sterility: FDA inspection found the recalled products were produced in a manner than cannot guarantee the sterility of the products purported to be sterile.
Vital Care Compounder is recalling moxefloxacin syrup products because FDA inspections found they weren't made with enough care to stay sterile. This means the medicine could be contaminated, which might cause infections if used.
The FDA found the products weren't made with enough care to stay sterile. This means the medicine could be contaminated with bacteria or other harmful substances, which might cause infections if used.
Prescription patients using the recalled moxefloxacin syrup. Those with compromised immune systems or open wounds are at slightly higher risk of infection.
Check for lot number 66470, produced between November 2022 and the date on the label. The product is a 1 mL syringe of moxefloxacin syrup, 0.15 mg per 0.1 mL, for prescription use only.
Look for lot number 66470 on the syringe label, which was produced around November 2022.
The FDA found the products weren't made with enough care to stay sterile, so they may be contaminated. Do not use these products.
Check for lot number 66470 on the syringe label, which was produced around November 2022.
The recall doesn't specify a remedy, so contact your healthcare provider for advice on safe alternatives.
We’ve drafted a message you can send Vital Care Compounder to request your refund or repair — edit it as you like.
Subject: Recall D-0040-2023 — Vital Care Compounder Vital Care Compounder Hello, I own a Vital Care Compounder that is covered by recall D-0040-2023 from Vital Care Compounder. 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.
