Angiodynamics recalls CAN 5F DUAL XCE: Bacterial endotoxins in some kits may cause fever or infection. Check catalog number 60M701532 for affected units.
A component of the kits might contain unsafe levels of bacterial endotoxins (pyrogens).
Angiodynamics is recalling certain CAN 5F DUAL XCELA PICC kits due to potential bacterial endotoxins that could cause fever or infection. This is a safety issue for patients using these medical devices.
The kits might contain unsafe levels of bacterial endotoxins (pyrogens) that can cause fever or infection when used medically. This is a potential health risk for patients receiving the device.
Patients using the CAN 5F DUAL XCELA PICC kits with catalog number 60M701532 are affected. Healthcare providers who administer these kits may also be at risk.
Check for the catalog number 60M701532 on the kit packaging. The product was sold with lot numbers 5300582 or 5312582.
Look for the catalog number 60M701532 on the kit packaging to confirm if it's affected.
The recall is for potential bacterial endotoxins that could cause fever or infection, but the risk level is low.
Check the catalog number 60M701532 on the kit packaging. Affected kits have lot numbers 5300582 or 5312582.
The recall does not specify a remedy, so contact Angiodynamics for guidance.
We’ve drafted a message you can send Angiodynamics to request your refund or repair — edit it as you like.
Subject: Recall Z-2219-2018 — Angiodynamics Angiodynamics Hello, I own a Angiodynamics that is covered by recall Z-2219-2018 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.
