FDAMarch 5, 2025device

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

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

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

What to do

FDA enforcement status: Ongoing

Brands named

medline industries lp northfieldmedlinemedline industries

UPCs

10080196415106

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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