Devices

Device Recall Terumo Analyzer, Ion, HydrogenIon (pH), BloodPhase, Indwelling

Model / Serial
Lots Affected: 2006-O6AD, 2006-O8AD, 2006-O8AP, 6O8AP6O8AD
Product Classification
Anesthesiology Devices
Device Class
2
Implanted device?
No
Distribution
Nationwide in CA, IL, MA, MD, NC, & OK; Internationally in Belgium & Kuwait
Product Description
TERUMO KHURI MYOCARDIAL PH MONITORING SYSTEM, CATALOG NUMBER 7205
Manufacturer
Terumo Cardiovascular Systems Corp
1 Event
- Recall of Device Recall Terumo Analyzer, Ion, HydrogenIon (pH), BloodPhase, Indwelling

Manufacturer

Terumo Cardiovascular Systems Corp

Manufacturer Address
Terumo Cardiovascular Systems Corp, 1311 Valencia Ave, Tustin CA 92780-6447
Manufacturer Parent Company (2017)
Terumo Corp.
Source
USFDA

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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