ClearanceBrief
Recall Z-0275-2013 ยท DTQ Console, Heart-Lung Machine, Cardiopulmonary Bypass

Sorin Group USA, Inc.

Sorin C5 Perfusion System, Item number 58-00-00 The Stockert S5/Sorin C5 System is intended to be used during cardiopulmonary bypass for procedures lasting six hours or less.

DateNov 8, 2012 (initiated Sep 19, 2012)
StatusTerminated
ReasonSorin Group USA, Inc. has issued an Urgent Field Safety Notice regarding certain serial numbers of the Sorin Group S5 Perfusion System due to reports of a "Fault in motor controller" alarm message displayed on the system panel. This could lead to unintended pump stoppage which may result in permanent impairment or life-threatening injury. An out of specification electrical component was determin
Root causeMixed-up of materials/components
ActionThe firm, Sorin Group, sent an "URGENT FIELD SAFETY NOTICE" dated September 19, 2012 to all affected customers by certified mail. The notice described the product, problem and actions to be taken. The customers were instructed to follow the provided instructions for the continued safe use of the Perfusion systems until they have been serviced or replaced by Sorin Group. The Sorin Group Service Team will contact the customer to schedule servicing and replacement of the affected product. The customers were also instructed to complete and return the Customer Response Form via fax to 303-467-65
Quantity2 units (no product distributed within the US).
DistributionWorldwide distribution: USA (nationwide) including states of: AZ, GA, MI, MS, NC, NY, PA, SC, and TX; and countries of: Austria, Australia, Belgium, Canada, People's Republic of China, Columbia, Denmark, Finland, Germany, India, Iran-Islamic Republic of, Ireland, Japan, Lebanon, Morocco, Pakistan, P
FDA recordOpen on fda.gov

510(k) clearances named in this recall

K071318MODIFICATION TO: STOCKERT S5 SYSTEM
Sorin Group Deutschland GmbH, Jul 6, 2007
K093882SORIN C5 SYSTEM MODEL 58-00-00
Sorin Group Deutschland GmbH, Jan 15, 2010