Angiodynamics recalls BioFlo PICC kits with potential bacterial endotoxins. Affected kits may cause fever or infection. Consumers should contact for details.
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 endotox: this could cause fever or infection in users. The recall affects specific kits sold with catalog number 75-038.
The kits might contain unsafe levels of bacterial endotoxins, which can cause fever or infection in users. This risk is specific to the kits with the listed catalog numbers and lots.
Healthcare workers using the recalled kits for PICC line procedures are most at risk. Patients receiving care with these kits could also be affected.
Check for the catalog number 75-038 on the kit. The affected lots are 5301462, 5316413, and 5320267. The kits are sold by Angiodynamics.
Look for catalog number 75-038 and affected lots: 5301462, 5316413, 5320267.
The recall is for potential bacterial endotoxins that could cause fever or infection, but the remedy is not stated in the record.
Check for catalog number 75-038 and affected lots: 5301462, 5316413, 5320267.
The recall record does not specify a remedy, so contact Angiodynamics for further instructions.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2224-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2224-2018 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.
