Angiodynamics recalls BioFlo Midline 5F DL-20cm MST-45 Kit with potential bacterial endotoxins. Affected kits may cause fever or infection if used in medical procedures.
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Angiodynamics recalls certain BioFlo Midline 5F kits due to possible unsafe levels of bacterial endotox: using these kits in medical procedures could cause fever or infection. This is a serious health risk for patients undergoing procedures.
The kits might contain unsafe levels of bacterial endotoxins (pyrogens) that can cause fever or infection when used in medical procedures. This is a serious health risk for patients undergoing procedures.
Medical professionals using the recalled BioFlo Midline 5F kits for procedures are at risk. Patients receiving these kits could develop fever or infection.
Check for the catalog number 46-810 on the kit. The kit includes two Nitinol guidewires and has the UPN H965468100 and lot number 5314926.
Immediately stop using the recalled BioFlo Midline 5F DL-20cm MST-45 Kit with catalog number 46-810.
The kits might contain unsafe levels of bacterial endotoxins (pyrogens) that could cause fever or infection in medical procedures.
Immediately stop using the kit and contact Angiodynamics for instructions.
The recall record does not mention a fix or remedy.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2199-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2199-2018 from Angiodynamics. 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.
