FDA Recall Terminated

Datascope System 98/98xt, CS 100/CS100i and CS 300 Intra-Aortic Balloon Pump. The Intra-Aortic Balloon Pump (IABP) is an electromechanical system used to inflate and deflate intra-aortic balloons in cardiovascular procedures.

Recall: Z-1523-2014 · Initiated March 21, 2014

Recall

Recall Number
Z-1523-2014
Event Number
67815
Firm
Maquet Datascope Corp Cardiac Assist Division
FEI Number
3001418283
Product Code
DSP
Status
Terminated
Root Cause
Nonconforming Material/Component
Initiated
March 21, 2014
Posted
May 21, 2014
Terminated
March 20, 2018
Address
1300 MacArthur Blvd., Mahwah, NJ, 07430-2052

Description

Datascope System 98/98xt, CS 100/CS100i and CS 300 Intra-Aortic Balloon Pump. The Intra-Aortic Balloon Pump (IABP) is an electromechanical system used to inflate and deflate intra-aortic balloons in cardiovascular procedures.

Reason

Potential mechanical failure of the fan assembly associated with the power supply. A fan assembly failure could result in the power supply overheating and cause the IABP to shut down without warning.

Action

Maquet Inc. sent an Urgent Medical Device Field Correction letter dated March 21, 2014, to all affected customers. The letter identified the affected product, problem, and actions to be taken.. Customers were instructed that their Service Representatiave would contact them to schedule the replacement of the fan assembly at no cost to the customer. Upon completion customers were requested to sign a service repair order to verify satisfactory completion of the work. Customers with questions within Puerto Rico, were instructed to contact Technical Support in Mexico at +52-55-9000-8970, ext 104. For questions regarding this recall call 973-709-7652. A field correction letter was sent out on April 15, 2014 to additional consignees that did not receive the March 15, 2014 letter. Maquet issued press on May 9, 2014.

Distribution

Worldwide Distribution - USA (nationwide) and approximately 104 countries.

Quantity

11,881 units (US 5183 and OUS 6698)