Product Wiki · Recalls · U.S. FDA — Device Enforcement

Recall Z-0624-2016 — NIPRO SET / SLIMLINE BLOOD TUBING SET for Hemodialysis with Transducer Protectors and Priming Set A disposable bloodline intended to provide extracorporeal access to the patient's blood during Hemodialysis. Compatible for use with Fresenius 2008H, 2008K/K2 and 2008T dialysis machines.

U.S. FDA — Device Enforcement · United States · 2015-03-30 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-0624-2016
Date of alert: 2015-03-30
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Nipro Medical Corporation
Product category: device
Product type: Devices

Reported risk: Blood foaming was found during evaluation of the product.

Primary source: https://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts

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ProductGuru indexes recall and safety-alert records from ~30 public agency registries. We are not lawyers, regulators or product-safety consultants. This page restates what the named agency published; consult the primary source above (or qualified counsel in your jurisdiction) before any commercial, medical or safety decision.

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