Assurance Infusion recalls Trimix Forte Plus 30mg/4mg/40mcg/ml vials due to lack of sterility assurance. Affected lots expired by 03/31/2020. Contact for details.
Lack of sterility assurance.
Assurance Infusion is recalling Trimix Forte Plus vials because they may not be sterile. This could lead to infections if used improperly. Patients should check their vial lot numbers and contact the manufacturer.
The vials may not be sterile, which can cause infections if injected. This is a serious risk for medical use but the exact mechanism isn't specified in the recall.
Patients using Trimix Forte Plus vials for medical treatments. Those with vials from the listed lots are most at risk.
Check the vial lot number on the packaging. Affected lots include 07032019@12 (exp. 12/30/2019), 08212019@32 (exp. 02/17/2020), and 10032019@12 (exp. 03/31/2020).
Look for the lot number on the vial packaging to determine if it's affected.
Assurance Infusion is recalling Trimix Forte Plus 30mg/4mg/40mcg/ml vials due to lack of sterility assurance.
Lots 07032019@12 (exp. 12/30/2019), 08212019@32 (exp. 02/17/2020), and 10032019@12 (exp. 03/31/2020).
Check the vial lot number on the packaging; affected lots are listed in the recall notice.
We’ve drafted a message you can send Assurance Infusion to request your refund or repair — edit it as you like.
Subject: Recall D-0778-2020 — Assurance Infusion Assurance Infusion Hello, I own a Assurance Infusion that is covered by recall D-0778-2020 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.
