Angiodynamics recalls BioFlo PICC nursing kits with possible bacterial endotoxins. Affected kits may cause fever or infection if used improperly.
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Angiodynamics is recalling BioFlo PIC: Nursing kits that might contain unsafe levels of bacterial endotoxins. This could lead to fever or infection if the kits are used.
The kits might contain unsafe levels of bacterial endotoxins (pyrogens) that could cause fever or infection in patients. This risk is specific to medical use where the kits are inserted into patients' bodies.
Nurses and healthcare workers using the BioFlo PICC kits for patient care. Patients receiving IV treatments through these kits may be at risk if the endotoxins cause infection.
Check for the catalog number 75-032 on the kit. The product was sold with UPN H965750325 and lot number 5312035.
Look for catalog number 75-032 on the kit packaging or label.
The recall states the kits might contain unsafe levels of bacterial endotoxins, which could cause fever or infection in patients. However, the risk is low and not all kits are affected.
Check for catalog number 75-032 on the kit. The product was sold with UPN H965750325 and lot number 5312035.
The recall does not specify a remedy, so contact Angiodynamics for guidance on next steps.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2222-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2222-2018 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.
