FDAClass IISeptember 11, 2019

Fujifilm FDR Go Plus mobile X-ray system recall

Fujifilm FDR Go Plus mobile X-ray system

Why was Fujifilm FDR Go Plus mobile X-ray system recalled?

The graphics driver of the FDR Go PLUS might cause the appearance of a Blue Screen of Death (BSoD)

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?

All serial numbers

Product
Fujifilm FDR Go Plus mobile X-ray system
Recalling firm
Fujifilm Medical Systems U.S.A., Inc.
Quantity
174 units
Distribution
Nationwide
Recall date
September 11, 2019
Classification
Class II
Status
Terminated
Agency
FDA (device)
Open FDA enforcement record Latest recalls