MEDLINE INDUSTRIES, LP - Northfield recalls MEDLINE ReNewal ENT Coblator II PROcise mAx,W/ Integrated Cable Suction & Saline (Blue), Item Number REF EICA88980R

Recalled April 16, 2025 · FDA recall Z-1549-2025 · MEDLINE INDUSTRIES, LP - Northfield

Hazard

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

Units

224 units

Sold at

US Nationwide distribution

Description

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

Product

MEDLINE ReNewal ENT Coblator II PROcise mAx,W/ Integrated Cable Suction & Saline (Blue), Item Number REF EICA88980R

Manufacturer(s)

MEDLINE INDUSTRIES, LP - Northfield

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →