medical Class II Updated 2019-03-27

Fujifilm Medical Systems U.S.A., Inc. recalls Fujifilm FDR Go PLUS, Mobile X-Ray System Product Usage:

Recalled Product

Fujifilm FDR Go PLUS, Mobile X-Ray System Product Usage: This device is intended to be used to take a film, CR or general radiography of patients in the hospital who cannot move and/or of outpatients in emergency. Exposure can be captured on film, CR or Digital Radiography (DR)>


Hazard / Issue

FUJIFILM Medical Systems U.S.A., Inc., Modality Systems became aware of the possibility that the braking mechanism might not be engaged in all cases when the driving handle has been released.

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Serial Numbers: MQ0001281001 through MQ0001285004
View official government recall

Looking for safe alternatives?

Browse certified-safe products in this category on Amazon →