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

Recall Z-2328-2017 — Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Catheter, Catheter, Percutaneous The Arrow Single-Lumen Catheter permits venous access to the central circulation

U.S. FDA — Device Enforcement · United States · 2017-05-09 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-2328-2017
Date of alert
2017-05-09
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 the affected product because the packaging may not be completely sealed, which may compromise sterility.
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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