Class II

Medical Device Recall: MEDLINE ReNewal ENT Coblator II PROcise XP Wand,w/Integrated Cable Suction & Saline (Blue), Item Number REF EICA88720R

MEDLINE INDUSTRIES, LP - Northfield · March 5, 2025

Reason for Recall

Medline ReNewal has identified that the drip chambers of affected devices may disconnect from the saline line tubing when under tension.

Distribution

US Nationwide distribution

States Affected

NATIONWIDE

Quantity Affected

315 units

Source: FDA (openFDA Device Enforcement)

Recall number: Z-1548-2025

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.