Angiodynamics recalls RS 5F DL XPP KIT (Catalog 60M183104) due to potential unsafe bacterial endotoxins. Affected kits may pose health risks if used improperly.
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Angiodynamics is recalling its RS 5F DL XPP K: kits that might contain unsafe levels of bacterial endotoxins (pyrogens). This could lead to health issues if the kits are used without proper precautions.
The kits might contain unsafe levels of bacterial endotoxins, which can cause fever or other health issues when introduced into the body. This risk is related to the medical use of the kit.
Users of the RS 5F DL XPP KIT with Catalog Number 60M183104 are affected. Patients undergoing medical procedures using this kit may be at higher risk.
Check for the catalog number 60M183104 on the kit. The kit was sold with UPN H96560M1831041 and lot number 5310755.
Verify the catalog number 60M183104 and lot number 5310755 on the kit.
The recall states the kits might contain unsafe levels of bacterial endotoxins, which could cause health issues if used improperly. However, the risk level is low.
The recall does not specify a remedy, so no action is required beyond checking the kit details.
Check for catalog number 60M183104, UPN H96560M1831041, and lot number 5310755 on the kit.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2213-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2213-2018 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.
