Class I

Medical Device Recall: Medline General Surgery Tray kits: 1) ARTERIAL LINE TRAY, Item Number ART600; 2) A LINE TRAY, Item Number ART690

MEDLINE INDUSTRIES, LP - Northfield · December 31, 2024

Reason for Recall

The catheter subassembly in the Integrated Arterial Catheter was manufactured with excess material on the catheter hub.

Distribution

US Nationwide.

States Affected

NATIONWIDE

Quantity Affected

58 kits

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0992-2025

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.