FDA Device recall Z-0019-2014

MX 16-Slice CT Scanner System

FDA Device
Class II
terminated
Published 2013-10-23

On 2013-10-23 the FDA classified a Class II recall of MX 16-Slice CT Scanner System by Philips Medical Systems Cleveland, citing A pinch point at the end of the table top can cause injury.

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-0019-2014
Classification	Class II
Status	terminated
Initiated	2013-07-22
Published	2013-10-23
Last updated	2026-09-13 11:53 UTC
Company	Philips Medical Systems Cleveland
Distribution	AL, AR, CA, FL, GA, IL, IN, KY, MS, NC, NJ, NV, NY, OH, PA, VA

Product

MX 16-Slice CT Scanner System. Used as a whole-body computed tomography X-Ray system.

Reason

A pinch point at the end of the table top can cause injury.

Identifiers

code_info	Model # 728131 510(k) K083498 Serial #: EP16E090001, EP16E090002, EP16E090003, EP16E090006, EP16E090009, EP16E09001… Model # 728131 510(k) K083498 Serial #: EP16E090001, EP16E090002, EP16E090003, EP16E090006, EP16E090009, EP16E090010, EP16E090011, EP16E090012, EP16E090013, EP16E090015, EP16E100001, EP16E100004, EP16E100006, EP16E100008, EP16E100010, EP16E100012, EP16E100013, EP16E100016, EP16E100017, EP16E100018, EP16E100019, EP16E100020, EP16E100021, EP16E100022, EP16E100023, EP16E100024, EP16E100025, EP16E100026, EP16E100028, EP16E100029, EP16E100031, EP16E100032, EP16E100033, EP16E100034, EP16E100035, EP16E100037, EP16E100038, EP16E100039, EP16E100041, EP16E100043, EP16E100044, EP16E100045, EP16E100046, EP16E100047, EP16E100049, EP16E100051, EP16E100052, EP16E100055, EP16E100056, EP16E100058, EP16E100059, EP16E100060, EP16E100062, EP16E100063, EP16E100067, EP16E100069, EP16E100070, EP16E100071, EP16E100072, EP16E100073, EP16E100074, EP16E100075, EP16E100076, EP16E100077, EP16E100078, EP16E100079, EP16E100081, EP16E100082, EP16E100083, EP16E100084, EP16E100085, EP16E100086, EP16E100087, EP16E

code_info

Model # 728131 510(k) K083498 Serial #: EP16E090001, EP16E090002, EP16E090003, EP16E090006, EP16E090009, EP16E09001…

Model # 728131 510(k) K083498 Serial #: EP16E090001, EP16E090002, EP16E090003, EP16E090006, EP16E090009, EP16E090010, EP16E090011, EP16E090012, EP16E090013, EP16E090015, EP16E100001, EP16E100004, EP16E100006, EP16E100008, EP16E100010, EP16E100012, EP16E100013, EP16E100016, EP16E100017, EP16E100018, EP16E100019, EP16E100020, EP16E100021, EP16E100022, EP16E100023, EP16E100024, EP16E100025, EP16E100026, EP16E100028, EP16E100029, EP16E100031, EP16E100032, EP16E100033, EP16E100034, EP16E100035, EP16E100037, EP16E100038, EP16E100039, EP16E100041, EP16E100043, EP16E100044, EP16E100045, EP16E100046, EP16E100047, EP16E100049, EP16E100051, EP16E100052, EP16E100055, EP16E100056, EP16E100058, EP16E100059, EP16E100060, EP16E100062, EP16E100063, EP16E100067, EP16E100069, EP16E100070, EP16E100071, EP16E100072, EP16E100073, EP16E100074, EP16E100075, EP16E100076, EP16E100077, EP16E100078, EP16E100079, EP16E100081, EP16E100082, EP16E100083, EP16E100084, EP16E100085, EP16E100086, EP16E100087, EP16E

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-0019-2014%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.