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Recall Observatory FDA recall evidence

Device product

System 8000 Base Product Usage: The Sarns Modular Perfusion System 8000 is indicated for use for up to 6 hours on the extracorporeal circulation of blood for arterial perfusion, regional perfusion, and cardiopulmonary bypass procedures, when used by a qualified medical professional who is experienced in the operation of this or similar equipment.

Z-2218-2012

June 20, 2012

Class III

Product summary

Firm
Terumo Cardiovascular Systems Corporation
Event
Event 62732
Status
Terminated
Classification
Class III
Quantity
3
Official record key
device-enforcement:Z-2218-2012

Official wording

Reason: During a retrospective review of complaint events, TCVS identified on 06/15/12 that three (3) Sarns" System 8000 bases were manufactured and distributed from 11/13/06-11/29/06 with an incorrect incorrect amperage rating identified on the name plate label. The mislabeling was identified in January 2007 a set up process of the automark label printer. All units were corrected in the field in Marc

Code information: catalog number: 16401 and serial number: 2001, 2002, and 2003.

Distribution pattern: US Nationwide Distribution - including the state of New York

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    mislabeling