|
Product Description
|
Recall Class
|
FDA Recall Posting Date
|
Recalling Firm
|
Z-1730-2013 - CDI Blood Parameter Monitoring System 500 with Arterial and Venous blood parameter modules and Hematocrit/Saturation probe.
Intended for use during cardiopulmonary bypass procedures when continuous...
|
2
|
07/13/2013
|
Terumo Cardiovascular Systems Corporation
|
Z-1732-2013 - CDI Blood Parameter Monitoring System 500 with Arterial and Venous blood parameter modules.
Intended for use during cardiopulmonary bypass procedures when continuous monitoring of arterial and/or ven...
|
2
|
07/13/2013
|
Terumo Cardiovascular Systems Corporation
|
Z-1733-2013 - CDI Blood Parameter Monitoring System 500 with Arterial blood parameter module.
Intended for use during cardiopulmonary bypass procedures when continuous monitoring of arterial and/or venous pH, PC...
|
2
|
07/13/2013
|
Terumo Cardiovascular Systems Corporation
|
Z-1731-2013 - CDI Blood Parameter Monitoring System 500 with Arterial blood parameter modules and Hematocrit/Saturation probe.
Intended for use during cardiopulmonary bypass procedures when continuous monitorin...
|
2
|
07/13/2013
|
Terumo Cardiovascular Systems Corporation
|
Z-1734-2013 - CDI Blood Parameter Monitoring System 500 with Venous blood parameter module.
Intended for use during cardiopulmonary bypass procedures when continuous monitoring of arterial and/or venous pH, PCO2...
|
2
|
07/13/2013
|
Terumo Cardiovascular Systems Corporation
|