Angiodynamics recalls RS 5F DL BIOFLO PASV kits with possible unsafe bacterial endotoxin levels. Affected kits may cause fever or infection if used improperly.
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Angiodynamics recalls certain RS 5F DL BIOFLO PASV kits due to potential unsafe levels of bacterial endotoxins. Using these kits could cause fever or infection in some people.
The kits might contain unsafe levels of bacterial endotoxins, which can cause fever or infection if the product is used improperly. This is a risk during medical procedures where the kits are used.
People who own or use the recalled RS 5F DL BIOFLO PASV kits for medical procedures. Those with compromised immune systems may be at higher risk.
Check for the catalog number 60M132324 on the kit packaging. The product was sold with UPN H96560M1323241 and lot number 5312922.
Look for the catalog number 60M132324 on the kit packaging to confirm if it is affected.
The kits might contain unsafe levels of bacterial endotoxins, which can cause fever or infection if used improperly.
Check for the catalog number 60M132324 on the kit packaging. The product was sold with UPN H96560M1323241 and lot number 5312922.
The recall does not require immediate stop use; check the catalog number to confirm if affected.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2205-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2205-2018 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.
