Angiodynamics recalls RS 5F DL XCELA PICC kits with potential bacterial endotoxins. Affected units have catalog number 60M122272. Contact for remedy details.
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Angiodynamics is recalling certain PICC kits that may contain unsafe levels of bacterial endotox: pyrogens. This could cause fever or infection in patients. The recall affects specific kits sold with catalog number 60M122272.
The kits might contain unsafe levels of bacterial endotoxins (pyrogens). These substances can cause fever or infection in patients if they enter the bloodstream.
Patients using the recalled PICC kits are most at risk. Healthcare providers who have the kits may also be affected.
Check for the catalog number 60M122272 on the kit packaging. The recall covers specific units with UPN: M00160M1222721 and Lot: 5312021.
Look for catalog number 60M122272 on the kit packaging.
Angiodynamics recalls RS 5F DL XCELA PICC kits with potential unsafe levels of bacterial endotoxins (pyrogens).
Check for catalog number 60M122272 on the kit packaging. The recall covers units with UPN: M00160M1222721 and Lot: 5312021.
The recall record does not specify a remedy, so contact Angiodynamics for instructions.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2225-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2225-2018 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.
