FDA Device recall Z-1064-2015

Digital Mobile X-ray Systems used to take diagnostic radiographic exposures or patients

FDA Device
Class II
terminated
Published 2015-02-18

On 2015-02-18 the FDA classified a Class II recall of Digital Mobile X-ray Systems used to take diagnostic radiographic exposures or patients by Virtual Imaging, citing there is a potential for unintended and erratic motion.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1064-2015
Classification	Class II
Status	terminated
Initiated	2014-09-22
Published	2015-02-18
Last updated	2026-09-13 11:53 UTC
Company	Virtual Imaging
Distribution	US

Product

Digital Mobile X-ray Systems used to take diagnostic radiographic exposures or patients.

Reason

There is a potential for unintended and erratic motion.

Identifiers

code_info	1) Model: MOBILE 32KW ANALOG; Serial Numbers: G29393 , G29395 , G29404 , G30236 , G30258 , G33309 , G33344 , G38… 1) Model: MOBILE 32KW ANALOG; Serial Numbers: G29393 , G29395 , G29404 , G30236 , G30258 , G33309 , G33344 , G38069 , G38082 , G38711 , G38712 , G40196 , G40590 , G40989 , G41143 , G41163 , G60166 , G60169 , G60461 , G62020; 2) Model: MOBILE 40KW; Serial Numbers: G33126 , G35630 , G35641 , G35718 , G37357 , G31259; 3) Model: MOBILE 40KW 50G; Serial Numbers: G30684; 4) Model: MOBILE 40KW 55C; Serial Numbers: G37528; 5) Model: MOBILE 40KW 70C; Serial Numbers: G36211 , G36227 , G36281 , G36573 , G36581 , G36626 , G37168 , G38613 , G39518 , G40190 , G40227 , G60432 , G60435 , G60518 , G61367 , G61368 , G61720 , G61725 , G61726; 6) Model: MOBILE 40KW ANALOG; Serial Numbers: G30240; 7) Model: MOBILE2 40KW 50C; Serial Numbers: G31414 , G32487; 8) Model: MOBILE2 40KW 50G; Serial Numbers: G29416 , G29426 , G29824 , G29873 , G29878 , G30025 , G30155 , G30156 , G30160 , G30165 , G30173 , G30570 , G30685 , G30689 , G30761 , G3

code_info

1) Model: MOBILE 32KW ANALOG; Serial Numbers: G29393 , G29395 , G29404 , G30236 , G30258 , G33309 , G33344 , G38…

1) Model: MOBILE 32KW ANALOG; Serial Numbers: G29393 , G29395 , G29404 , G30236 , G30258 , G33309 , G33344 , G38069 , G38082 , G38711 , G38712 , G40196 , G40590 , G40989 , G41143 , G41163 , G60166 , G60169 , G60461 , G62020; 2) Model: MOBILE 40KW; Serial Numbers: G33126 , G35630 , G35641 , G35718 , G37357 , G31259; 3) Model: MOBILE 40KW 50G; Serial Numbers: G30684; 4) Model: MOBILE 40KW 55C; Serial Numbers: G37528; 5) Model: MOBILE 40KW 70C; Serial Numbers: G36211 , G36227 , G36281 , G36573 , G36581 , G36626 , G37168 , G38613 , G39518 , G40190 , G40227 , G60432 , G60435 , G60518 , G61367 , G61368 , G61720 , G61725 , G61726; 6) Model: MOBILE 40KW ANALOG; Serial Numbers: G30240; 7) Model: MOBILE2 40KW 50C; Serial Numbers: G31414 , G32487; 8) Model: MOBILE2 40KW 50G; Serial Numbers: G29416 , G29426 , G29824 , G29873 , G29878 , G30025 , G30155 , G30156 , G30160 , G30165 , G30173 , G30570 , G30685 , G30689 , G30761 , G3

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:53 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1064-2015%22

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