FDAMay 15, 2015device

EVAC 70 XTRA with Integrated Cable REF EICA5872-01 Product Usage: PLASMA WAND devices are indicated for ablation, resection, and coagulation of soft tissue and hemostasis of blood vessels in otorhinolaryngology (ENT) surgery including: adenoidectomy, cysts, head, neck, oral, and sinus surgery, ma...

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

The hazard

Potential component failure causing device inoperability

What to do

FDA enforcement status: Terminated

Brands named

arthrocare medicalarthrocare

Recall history

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

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