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

Recall Z-2327-2017 — Arterial Catheterization Kit, Arterial Line Kit with Sharps Safety Features wire, guide, catheter The Arrow Arterial Catheterization device permits access to the peripheral arterial circulation or to other small vessels

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-2327-2017
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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