Angiodynamics recalls BioFlo PICC (Valved) 5FDL- 55cm Maximal Barrier Nursing Kits with potential bacterial endotoxins. Consumers should check catalog numbers 75-019 for affected units.
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Angiodynamics is recalling BioFlo PICC (Valved) 5FDL-55cm Maximal Barrier Nursing Kits due to possible unsafe levels of bacterial endotoxins. This could cause fever or infection if used improperly.
The kits might contain unsafe levels of bacterial endotoxins (pyrogens) that can cause fever or infection when used in medical procedures. This risk is specific to the kits' intended medical use.
Nurses and healthcare providers who use BioFlo PICC kits for patient care. Those with the catalog number 75-019 are most at risk.
Check the catalog number on the kit, which is 75-019. The kits were sold with lot numbers 5301073 or 5304893.
Look for the catalog number 75-019 on the kit packaging.
The recall is for potential bacterial endotoxins that could cause fever or infection, but the risk is low if used properly.
Check the catalog number on the kit, which is 75-019. The kits were sold with lot numbers 5301073 or 5304893.
The recall does not specify a remedy, so contact Angiodynamics for guidance.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2221-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2221-2018 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.
