FDAClass IIMarch 22, 2017

OEC FlexiView 8800 recall

OEC FlexiView 8800, Digital Mobile Imaging System, GE Medical Systems

Why was OEC FlexiView 8800 recalled?

OEC FlexiView 8800 workstation power cable assembly issue which can result in a loss of imaging functionality due to intermittent power cord failures.

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?

OEC FlexiView 8800 systems that had NEMA 5-15 15 Amp power cords replaced between January 28, 2016 and November 23, 2016.

Product
OEC FlexiView 8800, Digital Mobile Imaging System, GE Medical Systems
Recalling firm
GE OEC Medical Systems, Inc
Quantity
1
Distribution
One consignee in CA.
Recall date
March 22, 2017
Classification
Class II
Status
Terminated
Agency
FDA (device)
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