RecallDepth

Terumo 100/120V AC, Advanced Perfusion System Platform (APS) for use in cardiopulmonary bypass procedures. Catalog Number 801763

Company
Terumo Cardiovascular Systems Corporation
Recall Initiated
August 28, 2018
Terminated
April 23, 2020
Recall Number
Z-3242-2018
Quantity
47 units
Firm Location
Ann Arbor, MI

Reason for Recall

Screws on a Terumo Advanced Perfusion System 1 Power Manager Board (the base unit circuit board) were not torqued to specification. It is possible that a screw which has not been properly torqued can go undetected during manufacturing testing and may loosen over time, resulting in the potential for an electrical short in the system.

Distribution

Nationwide Foreign: Mexico, BELGIUM, CANADA, India, Indonesia, Singapore, South Korea , Vietnam

Lot / Code Info

Serial Numbers: 0386  1481  1497  1509  1526  1529  1531  1532  1535  1536  1537  1538  1539  1540  1541  1542  1543  1544  1545  1546  1548  1549  1550  1551  1552  1553  1554  1555  1556  1557  1558  1561  1562  1563  1564  1565  1566  1570  1597  1612  1630  1631  1640  1641  1649  1547  1560  1559  1567  Spare Parts:  870509 ASSEMBLY POWER MANAGER POD APS S/N: 03130 , 03308

Root Cause

Process control

Action Taken

Terumo CVS issued letter on 8/2/818 via Fed'X 2 day air to inform users of the problem for the Power Manager boards with unverifiable or out of specification screws, potential hazard and field correction. A Terumo Field Service Representative will contact users to schedule the field correction activities. Terumo CVS Customer Service: 1.800.521.2818, Monday Friday, 8 a.m. 6 p.m. ET

More recalls by Terumo Cardiovascular Systems Corporation

View all recalls by this company →