ClearanceBrief
Recall Z-0663-2010 ยท IOQ Bed, Flotation Therapy, Powered

KCI USA, Inc.

AC Power Cords, 110V Manufactured by Electri-Cord Manufacturing Company in Westfield, PA. Power Cord #4102204 used with Tricell 60601 Model 212857, First Step Select Model 215200 , and Plexipulse Model 205835.

DateJan 25, 2010 (initiated Nov 4, 2009)
StatusTerminated
ReasonPower cords may crack and fail inside plug with potential for fire hazard.
Root causeNonconforming Material/Component
ActionKinetics Concepts, Inc. (KCI) issued an "Urgent Medical Device Correction" letter dated November 4, 2009. Consignees were informed of the affected product and instructed to take necessary action to avoid any further issues associated with the product. For further information, contact KCI's technical support team at 1-800-275-4524 option #3.
Quantity10,520
DistributionNationwide and Canada
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K944567COWBOY X
Kinetic Concepts, Inc., Jun 21, 1995