Angiodynamics recalls RS 5F DL XPP kits with potential unsafe bacterial endotoxins. Affected kits may cause fever or infection if used improperly.
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Angiodynamics is recalling certain RS 5F DL XPP kits due to possible unsafe levels of bacterial endotox: this could lead to fever or infection if the kit is used incorrectly.
The kits might contain unsafe levels of bacterial endotoxins (pyrogens) that can cause fever or infection when used. This risk is related to improper use of the medical device.
Patients using the RS 5F DL XPP kits for medical procedures are most at risk. The recall applies to kits sold with specific catalog numbers and lot codes.
Check for the catalog number 60M030393 and lot numbers 5304317 on the kit packaging. The recall covers kits sold with these specific identifiers.
Look for catalog number 60M030393 and lot numbers 5304317 on the kit packaging.
The kits might contain unsafe levels of bacterial endotoxins (pyrogens) that could cause fever or infection if used incorrectly.
Check the catalog number and lot numbers on the packaging. If they match 60M030393 and 5304317, contact Angiodynamics for guidance.
The recall states potential fever or infection risks, but no specific serious injury mechanism is mentioned.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2201-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2201-2018 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.
