Angiodynamics recalls 5F DL BIOFLO PICC kits with potential bacterial endotoxins. Consumers should check catalog numbers and lot codes for affected units.
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Angiodynamics is recalling certain 5F DL BIOF:PICC 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, which can cause fever or infection when introduced into the bloodstream. This risk is typically low but requires careful handling.
Patients using the 5F DL BIOFLO PICC kits with catalog numbers 60M180592 and specific lot numbers are affected. Healthcare providers administering these kits are at higher risk.
Check the catalog number (60M180592) and lot numbers (5313507, 5316369, 5318603, 5321025) on the product packaging.
Look for catalog number 60M180592 and lot numbers 5313507, 5316369, 5318603, or 5321025 on the kit packaging.
The recall is for potential bacterial endotoxins that could cause fever or infection, but the risk is low and not all kits are affected.
Check the catalog number (60M180592) and lot numbers (5313507, 5316369, 5318603, 5321025) on the product packaging.
The recall does not specify a remedy, so contact Angiodynamics directly 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-2210-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2210-2018 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.
