RecallRadar

FDA Device recall Z-1754-2019

Precision 500D The Precision 500D R&F X-ray System is intended to be used as a universal diagnostic imaging system for radiographic and flu…

On 2019-06-19 the FDA classified a Class II recall of Precision 500D The Precision 500D R&F X-ray System is intended to be used as a universal diagnostic imaging system for radiographic and flu… by Ge Healthcare, citing there has been a reported incident of a Distar CRT monitor that has fallen off the monitor wall mount related to product aging.

Read the official FDA Device notice

AgencyFDA Device
Recall numberZ-1754-2019
ClassificationClass II
Statusterminated
Initiated2019-03-29
Published2019-06-19
Last updated2026-09-13 11:55 UTC
CompanyGe Healthcare
DistributionUS

Product

Precision 500D The Precision 500D R&F X-ray System is intended to be used as a universal diagnostic imaging system for radiographic and fluoroscopic examinations, including general R&F and pediatric examinations.

Reason

There has been a reported incident of a Distar CRT monitor that has fallen off the monitor wall mount related to product aging.

Identifiers

code_info
204787RF1; 205814RF1; 209826500D; 229P500RF2; 410448RF; 417682BRF; 506857P500; 519663PR500; 519685PR500; 561791RM2; 603…204787RF1; 205814RF1; 209826500D; 229P500RF2; 410448RF; 417682BRF; 506857P500; 519663PR500; 519685PR500; 561791RM2; 603668C5; 618635RF; 636625SJR1; 718630PRECISION; 770793KP500D2; 810326P500; 850494WF4; 903731PRP500; 985230DCRF4; and AM16KFZ328.

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1754-2019%22

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