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U.S. Department of Health and Human Services

Class 2 Device Recall Sorin S5 Perfusionn System

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 Class 2 Device Recall Sorin S5 Perfusionn Systemsee related information
Date Initiated by FirmSeptember 24, 2013
Date PostedNovember 04, 2013
Recall Status1 Terminated 3 on July 10, 2014
Recall NumberZ-0142-2014
Recall Event ID 66464
510(K)NumberK071318 
Product Classification Console, heart-lung machine, cardiopulmonary bypass - Product Code DTQ
ProductS5 Heart-lung machine, Stockert S5 System. Catalogue No: 48-30/40/50-00. The Stockert S5 System is intended to be used during cardiopulmonary bypass for procedures lasting six(6) hours or less.
Code Information Serial Numbers: 48E00235,48E00339,48E00342,48E01753,48E02767,48E02753,48E02745,48E02746,48E02748,48E02416,48E01033,480E1038,48E01040,48E01041,48E01043,48E01044,48E01051,48E02631,48E01183,48E02758,48E02764,48E01832,48E01834,48E02278,48E02722,48E02732,48E02326,48E02797,48E02793,48E02791,48E02781,48E02785,48E02786,48E02783,48E02772,48E02802,48E02778,48E02784,48E02788,48E02789,48E02779,48E02792,48E02790,48E02771,48E02773,48E02776,48E02799,48E02801
Recalling Firm/
Manufacturer		 Sorin Group Deutschland GmbH
Lindberghstrasse 25
Munchen Germany
For Additional Information ContactCheri Voorhees
303-467-6527
Manufacturer Reason
for Recall		Sorin Group is recalling certain models of S5 Perfusion Systems due to malfunction of cardioplegia control.
FDA Determined
Cause 2		Software Manufacturing/Software Deployment
ActionSorin Group sent an Urgent Field Safety Notice dated September 24, 2013, to all affected customers. The letter informed users of the potential for failing of automatic cardioplegia delivery function and notified them that they would be contacted by the Sorin Service Group to arrange an appointment to update the firmware on site. Customers were asked to complete the Response form to confirm they had received, read and understood the Field Notice. For questions regarding this recall call 303-467-6527.
Quantity in Commerce84
DistributionWorldwide Distribution - USA including WA, NY, VA, TN, SC, TX, CA, CO, MA, WI, MD, AL, ND, and Puerto Rico and Internationally to Italy, Finland, Germany, Sweden, and Great Britain.
Total Product Life CycleTPLC Device Report
1 A record in this database is created when a firm initiates a correction or removal action. The record is updated if the FDA identifies a violation and classifies the action as a recall, and it is updated for a final time when the recall is terminated. Learn more about medical device recalls.
2 Per FDA policy, recall cause determinations are subject to modification up to the point of termination of the recall.
3 For details about termination of a recall see Code of Federal Regulations (CFR) Title 21 §7.55.
510(K) Database510(K)s with Product Code = DTQ
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