Angiodynamics recalls BioFlo PICC kits with potential bacterial endotoxins. Affected kits may cause fever or infection if used. Contact for return instructions.
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Angiodynamics recalls certain BioFlo PICC nursing kits due to possible unsafe levels of bacterial endotoxins. Using these kits could lead to fever or infection in patients.
The kits might contain unsafe levels of bacterial end: endotoxins (pyrogens) that can cause fever or infection when used in medical procedures.
Healthcare workers using the recalled BioFlo PICC kits are most at risk. Patients receiving care with these kits may experience fever or infection.
Check for the catalog number 75-033 on the kit. The lot numbers 5310029 and 5310762 are also associated with this recall.
Look for the catalog number 75-033 and lot numbers 5310029 or 5310762 on the kit.
Angiodynamics recalls BioFlo PICC nursing kits with catalog number 75-033 that might contain unsafe levels of bacterial endotoxins.
Check for catalog number 75-033 and lot numbers 5310029 or 5310762 on the kit.
The recall record does not specify a remedy, so contact Angiodynamics directly for instructions.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2223-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2223-2018 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.
