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

Recall Z-0992-2025 — Medline General Surgery Tray kits: 1) ARTERIAL LINE TRAY, Item Number ART600; 2) A LINE TRAY, Item Number ART690

U.S. FDA — Device Enforcement · United States · 2024-12-31 · Class I

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Agency
U.S. FDA — Device Enforcement
Recall identifier
Z-0992-2025
Date of alert
2024-12-31
Country / jurisdiction
United States
Risk level
Class I
Risk type
recall
Brand
MEDLINE INDUSTRIES, LP - Northfield
Product category
device
Product type
Devices
Barcode (EAN/GTIN)
10653160312727
Reported risk: The catheter subassembly in the Integrated Arterial Catheter was manufactured with excess material on the catheter hub.
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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