OEC¿ UroView 2800. The UroView 2800 is designed to recall
OEC¿ UroView 2800. The UroView 2800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical. and…
Why was OEC¿ UroView 2800. The UroView 2800 is designed to 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Serial No: P4-0490-R and P6-0705-L
- Product
- OEC¿ UroView 2800. The UroView 2800 is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic, surgical. and…
- Recalling firm
- GE OEC Medical Systems, Inc
- Quantity
- 2
- Distribution
- Worldwide Distribution.
- Recall date
- November 19, 2014
- Classification
- Class II
- Status
- Terminated
- Agency
- FDA (device)