ClearanceBrief
Recall Z-1141-2014 ยท OMP Negative Pressure Wound Therapy Powered Suction Pump

KCI USA, INC.

PRE2001US: Prevena Incision Management Customizable System Box (US-ONLY) Product Usage: The Prevena Incision Management System is intended to manage the environment of surgical incisions that continue to drain following sutured or stapled closure by maintaining a closed environment and removing exudates via the application of negative pressure wound therapy.

DateMar 5, 2014 (initiated Jan 30, 2014)
StatusTerminated
ReasonPrevena Incisional Management System Kit/Dressing Connector - the male connector on the tubing is difficult to connect to the female connector on the Prevena canister tubing
Root causeNonconforming Material/Component
ActionKCL sent an Urgent Voluntary Medical Device Correction letter dated February 2014 to all affected customers. The letter identified the affected product, problem and actions to be taken. Customers were instructed to locate, quarantine and return the affected device. For a replacement of the affected product and questions customers were instructed to contact KCL Customer Technical Support at 1-800-275-4524. A Product Reconciliation Form is attached to be completed and returned.
Quantity20,850 units total
DistributionUSA Nationwide Distribution
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K100821PREVENA INCISION MANAGEMENT SYSTEM
Kci USA, Inc., Jun 11, 2010
K123878PREVENA INCISION MANAGEMENT SYSTEM WITH CUSTOMIZABLE DRESSING
Kci USA, Inc. (Kinetic Concepts, Inc.), Jan 15, 2013