Class II

Medical Device Recall: MAHURKAR" Acute High Pressure Triple Lumen Catheter Tray Curved Extensions with IC Components: 12 Fr/Ch (4.0 mm) x 16 cm;

Mozarc Medical US LLC · October 17, 2025

Reason for Recall

A potential issue with the seal integrity of header bag packaging.

Distribution

US Nationwide distribution.

States Affected

NATIONWIDE

Quantity Affected

3,258 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-0422-2026

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.