Class II

Medical Device Recall: namic convenience kits labeled as: PML,72,ADULT,FLL-MLL,-,OEM, REF 80641722; medical convenience kit

MEDLINE INDUSTRIES, LP - Northfield · February 12, 2025

Reason for Recall

The female luer fittings on the Pressure Monitoring Lines (PMLs) were manufactured with excess material near the fluid pathway.

Distribution

Worldwide distribution - US Nationwide and the countries of The Netherlands, New Zealand, Slovakia

States Affected

NATIONWIDE

Quantity Affected

4400 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1428-2025

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.