FDAMarch 5, 2025device

MEDLINE ReNewal Coblator II ENT Evac 70 Xtra HP,w/Integrated Cable (Blue/Grey), Number REF EICA58740R

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

10888277395367

Recall history

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

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