Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
PROcise XP Wand with Integrated Cable REF EICA8872-01 Product Usage: Recalled by ArthroCare Medical Corporation Due to Potential component failure resulting in inoperability
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 Medical Corporation directly.
Affected Products
PROcise XP Wand with Integrated Cable REF EICA8872-01 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, mastoidectomy, myringotomy with effective hemorrhage control, nasal airway obstruction by 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: 2,355 units
Why Was This Recalled?
Potential component failure resulting in inoperability
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About ArthroCare Medical Corporation
ArthroCare Medical 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