FDA Device recall Z-1759-2015

MX 16 Slice (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems

FDA Device
Class II
terminated
Published 2015-06-17

On 2015-06-17 the FDA classified a Class II recall of MX 16 Slice (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems by Philips Medical Systems Cleveland, citing the firm was notified that the failure of the UPS accessory devices used in conjunction with Computed Tomography X-ray systems and Diagnostic Imaging systems. may result in batter….

Read the official FDA Device notice

Agency	FDA Device
Recall number	Z-1759-2015
Classification	Class II
Status	terminated
Initiated	2015-03-06
Published	2015-06-17
Last updated	2026-09-13 11:53 UTC
Company	Philips Medical Systems Cleveland
Distribution	US

Product

MX 16 Slice (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems.

Reason

The firm was notified that the failure of the UPS accessory devices used in conjunction with Computed Tomography X-ray systems and Diagnostic Imaging systems. may result in battery acid leakage, overheating and/or emission of fumes.

Identifiers

code_info	Model #: 728131; Serial #s: EP16E130006, EP16E130007, EP16E130009, EP16E130010, EP16E130012, EP16E130013, EP16E130014,… Model #: 728131; Serial #s: EP16E130006, EP16E130007, EP16E130009, EP16E130010, EP16E130012, EP16E130013, EP16E130014, EP16E130015, EP16E130016, EP16E130017, EP16E130020, EP16E130021, EP16E130022, EP16E130023, EP16E130025, EP16E130026, EP16E130027, EP16E130029, EP16E130030, EP16E130031, EP16E130033, EP16E130034, EP16E130035, EP16E130036, EP16E130037, EP16E130040, EP16E130041, EP16E130042, EP16E130043, EP16E130044, EP16E130045, EP16E130046, EP16E130047, EP16E130048, EP16E130049, EP16E130050, EP16E130051, EP16E130052, EP16E130053, EP16E130055, EP16E130056, EP16E130057, EP16E130058, EP16E130062, EP16E130063, EP16E130064, EP16E130065, EP16E130066, EP16E130067, EP16E130068, EP16E130069, EP16E130070, EP16E130071, EP16E130072, EP16E130073, EP16E130074, EP16E130075, EP16E130077, EP16E130078, EP16E130079, EP16E130080, EP16E130082, EP16E130083, EP16E130086, EP16E130087, EP16E130088, EP16E130089, EP16E130092, EP16E130093, EP16E130094, EP16E130095, EP16E130097, EP16E130098, EP16E130099, EP16E13010

code_info

Model #: 728131; Serial #s: EP16E130006, EP16E130007, EP16E130009, EP16E130010, EP16E130012, EP16E130013, EP16E130014,…

Model #: 728131; Serial #s: EP16E130006, EP16E130007, EP16E130009, EP16E130010, EP16E130012, EP16E130013, EP16E130014, EP16E130015, EP16E130016, EP16E130017, EP16E130020, EP16E130021, EP16E130022, EP16E130023, EP16E130025, EP16E130026, EP16E130027, EP16E130029, EP16E130030, EP16E130031, EP16E130033, EP16E130034, EP16E130035, EP16E130036, EP16E130037, EP16E130040, EP16E130041, EP16E130042, EP16E130043, EP16E130044, EP16E130045, EP16E130046, EP16E130047, EP16E130048, EP16E130049, EP16E130050, EP16E130051, EP16E130052, EP16E130053, EP16E130055, EP16E130056, EP16E130057, EP16E130058, EP16E130062, EP16E130063, EP16E130064, EP16E130065, EP16E130066, EP16E130067, EP16E130068, EP16E130069, EP16E130070, EP16E130071, EP16E130072, EP16E130073, EP16E130074, EP16E130075, EP16E130077, EP16E130078, EP16E130079, EP16E130080, EP16E130082, EP16E130083, EP16E130086, EP16E130087, EP16E130088, EP16E130089, EP16E130092, EP16E130093, EP16E130094, EP16E130095, EP16E130097, EP16E130098, EP16E130099, EP16E13010

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-1759-2015%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.