Angiodynamics recalls RS 5F DL BIOFLO PASV kits with potential unsafe bacterial endotoxins. Affected kits may cause fever or infection. Consumers should check catalog numbers and lot dates.
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Angiodynamics recalls certain RS 5F DL BIOF: PASV kits due to possible unsafe levels of bacterial endotoxins. This could cause fever or infection in users. The recall affects kits with specific catalog numbers and lot dates.
The kits might contain unsafe levels of bacterial endotoxins, which can cause fever or infection in users. This is a potential health risk if the endotoxins are present in the kit.
Users of the RS 5F DL BIOFLO PASV kits with catalog number 60M181578 and lot numbers 5303172 or 5310562 are affected. Patients receiving these kits for medical procedures are most at risk.
Check for catalog number 60M181578 and lot numbers 5303172 or 5310562 on the kit packaging. The kits were sold with UPN: H96560M1815781.
Look for catalog number 60M181578 and lot numbers 5303172 or 5310562 on the kit packaging.
The kits might contain unsafe levels of bacterial endotoxins, which can cause fever or infection.
Check for catalog number 60M181578 and lot numbers 5303172 or 5310562 on the kit packaging.
The recall record 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-2211-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2211-2018 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.