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

Recall Z-1166-2018 — ARROWg+ard Blue PLUS Pressure Injectable Multi-Lumen CVC Kit. Intended to permit venous access to the central circulation.

U.S. FDA — Device Enforcement · United States · 2017-11-14 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1166-2018
Date of alert
2017-11-14
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Arrow International Inc
Product category
device
Product type
Devices
Reported risk: Products do not contain the Central Venous Catheter Placement Procedures Note or the Central Line Insertion Checklist, which is a tool intended to guide clinicians in the use of best practices during central line insertions.
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.

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