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

Recall Z-1333-2018 — ARROWg+ard Blue¿ CVC Kit (1) Part Number (PN): CDC-24301-1A, (2) PN: CDC-24306-1A; (3) ARROWg+ard Blue¿ Large-Bore Multi-Lumen CVC Kit, PN: CDC-22123-1A; (4) Central Venous Catheterization Kit with Blue FlexTip(R) ARROWg+ard Blue(R) Catheter, Sharps Safety Features, and Maximal Barrier Precautions,

U.S. FDA — Device Enforcement · United States · 2017-12-22 · Class II

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-1333-2018
Date of alert
2017-12-22
Country / jurisdiction
United States
Risk level
Class II
Risk type
recall
Brand
Arrow International Inc
Product category
device
Product type
Devices
Reported risk: Certain lots of cardiovascular catheters may not be completely sealed and so sterility of the product cannot be guaranteed.
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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