Assurance Infusion recalls QUADMIX FORTE 1mL vials due to lack of sterility assurance. This could lead to infections if used improperly. Contact for details.
Lack of sterility assurance.
Assurance Infusion is recalling QUADMIX FORTE 1mL vials because they lack sterility assurance. Using these vials could lead to infections if the product is not properly handled.
The vials do not have proper sterility assurance, which means they could be contaminated. If used without proper sterilization, this could lead to infections in patients.
Patients using QUADMIX FORTE 1mL vials for medical treatments. Those with compromised immune systems may be at higher risk.
Check for the lot number 08132019@15 and expiration date 02/09/2020 on the vial. The product is sold by Assurance Infusion.
Look for the lot number 08132019@15 and expiration date 02/09/2020 on the vial.
QUADMIX FORTE 1mL vials from Assurance Infusion.
Due to lack of sterility assurance, which could lead to infections if used improperly.
Check for the lot number 08132019@15 and expiration date 02/09/2020 on the vial.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0765-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0765-2020 from Assurance Infusion. 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.
