Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
EVac 70 XTRA with Integrated Cable and PROcise EZ View Recalled by ArthroCare Corporation Due to Wands inspected with the adaptor fixture were released...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact ArthroCare Corporation directly.
Affected Products
EVac 70 XTRA with Integrated Cable and PROcise EZ View with Integrated Cable 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, mastoidectomy, myringotomy with effective hemorrhage control, nasal airway obstruction be reduction of hypertrophic nasal turbinates, nasopharyngeal/laryngeal indications including tracheal procedures, laryngeal polypectomy, and laryngeal lesion debulking, neck mass, papilloma keloids, submucosal palatal shrinkage, submucosal tissue shrinkage, tonsillectomy (including palatine tonsils), traditional uvulopalatoplasty (RAUP), tumors, and tissue in the uvula/soft palate for the treatment of snoring. It is intended for procedures using a conductive media, such as normal saline or Ringers lactate.
Quantity: 733 devices
Why Was This Recalled?
Wands inspected with the adaptor fixture were released to the field not meeting the dielectric (Hipot) specifications.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About ArthroCare Corporation
ArthroCare Corporation has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Device). Last updated March 26, 2026. View original report