Angiodynamics recalls RS 5F DL BIOFLO PASV kits with potential unsafe bacterial endotoxins. Affected units may cause fever or infection; contact for return instructions.
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Angiodynamics recalls certain blood flow kits due to possible unsafe levels of bacterial endotoxins in the product. This could lead to fever or infection in users, so affected individuals should stop using the kits and contact the manufacturer.
The kits might contain unsafe levels of bacterial endotoxins, which are substances that can cause fever or infection when introduced into the body. This risk is specific to the product's use in medical procedures.
Users of the RS 5:5F DL BIOFLO PASV blood flow kits with catalog number 60M161567 are affected. Patients undergoing medical procedures using these kits are most at risk.
Check for the catalog number 60M161567 on the kit packaging. The product was sold with UPN H96560M1615671 and lot number 5316086.
Immediately stop using the RS 5F DL BIOFLO PASV kit if it has the catalog number 60M161567.
The recall states there might be unsafe levels of bacterial endotoxins, which could cause fever or infection. However, the risk level is low.
Check the catalog number on the kit packaging; affected units have catalog number 60M161567.
Stop using the kit immediately and contact Angiodynamics for instructions on returning it.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2209-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2209-2018 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
