Series OEC 9800. The Series OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient,during diagnostic, surgical and interventional procedures.
Reported: November 19, 2014 Initiated: October 3, 2014 #Z-0195-2015
Product Description
Series OEC 9800. The Series OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient,during diagnostic, surgical and interventional procedures.
Reason for Recall
GE Healthcare initiated a field correction because prior revision of components were potentially installed on certain OEC 9800, FlexiView 8800, OEC MiniView 6800 and OEC UroView 2800 systems.
Details
- Recalling Firm
- GE OEC Medical Systems, Inc
- Units Affected
- 311
- Distribution
- Worldwide Distribution.
- Location
- Salt Lake City, UT
Frequently Asked Questions
What product was recalled? ▼
Series OEC 9800. The Series OEC 9800 is designed to provide fluoroscopic and spot-film imaging of the patient,during diagnostic, surgical and interventional procedures.. Recalled by GE OEC Medical Systems, Inc. Units affected: 311.
Why was this product recalled? ▼
GE Healthcare initiated a field correction because prior revision of components were potentially installed on certain OEC 9800, FlexiView 8800, OEC MiniView 6800 and OEC UroView 2800 systems.
Which agency issued this recall? ▼
This recall was issued by the FDA Devices on November 19, 2014. Severity: Moderate. Recall number: Z-0195-2015.
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