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

Recall Z-1879-2017 — Pressure Injectable Arrowg+ard Blue Plus Multi-Lumen Central Venous Catheterization Kit. Permits venous access to central circulation by way of subclavian, jugular and femoral veins. The ARROWg+ard technology is intended to provide protection against catheter-related bloodstream infections (CRBSIs)

U.S. FDA — Device Enforcement · United States · 2017-03-17 · Class II

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Agency: U.S. FDA — Device Enforcement
Recall identifier: Z-1879-2017
Date of alert: 2017-03-17
Country / jurisdiction: United States
Risk level: Class II
Risk type: recall
Brand: Arrow International Inc
Product category: device
Product type: Devices

Reported risk: Arrow International is recalling due to possible voids in the catheter hub, which could lead to an interlumen crossover.

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

Verify each fact at the issuing agency before acting. Recall scope, affected lots, and remediation instructions may be updated by the agency after our last sync.

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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