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ArthroCare Medical Recalls
5 recalls on record · January 15, 2014 to July 1, 2015 · Medical Devices
Recalls by year
14
15
Count of recall notices naming this brand, by the year the recall was announced. A quiet year is not proof of a safe year.
July 1, 2015Medical DevicesFDA
ArthroCare Medical Corporation recalls PROcise XP Wand with Integrated Cable REF EICA8872-01 Product Usage: PLASMA WAND devices are indicated for ablation,
Hazard: Potential component failure resulting in inoperability
July 1, 2015Medical DevicesFDA
ArthroCare Medical Corporation recalls EVAC 70 XTRA with Integrated Cable REF EICA5872-01 Product Usage: PLASMA WAND devices are indicated for ablation, re
Hazard: Potential component failure causing device inoperability
April 1, 2015Medical DevicesFDA
ArthroCare Medical Corporation recalls Coblator II System, 120V. Product Usage: The Coblator II (Model RF8000E) is a bipolar, radiofrequency electrosurgic
Hazard: The recalling firm was notified by the contract manufacturer that they had reversed the L2, L3, L4, or L5 components on the P/N09010 RoHS boards of the Coblator II Controller (Model RF8000E).
December 17, 2014Medical DevicesFDA
ArthroCare Medical Corporation recalls Model Number ASHA4730-01: Ambient HipVac 50 Wand with Integrated Finger Switches and Model Number ASHA5050-01: Ambient K
Hazard: Potential breach of sterile barrier due to defective product tray.
January 15, 2014Medical DevicesFDA
ArthroCare Medical Corporation recalls Arthrocare SPORTS MEDICINE, Knot Pusher, REF 25-3011, LOT #1049402, CON 1, 2013-10, NON-STERILE, Rx only
Hazard: A sharp edge on the cannulated tip of the device may damage or cut a suture.