FDA Device recall Z-1769-2015

iCT SP (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 iCT SP (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-1769-2015
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

iCT SP (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 #: 728311; Serial #s: 200021, 200022, 200023, 200024, 200025, 200026, 200027, 200029, 200030, 200031, 200032, 200… Model #: 728311; Serial #s: 200021, 200022, 200023, 200024, 200025, 200026, 200027, 200029, 200030, 200031, 200032, 200033, 200034, 200035, 200036, 200037, 200038, 200039, 200040, 200041, 200042, 200043, 200044, 200045, 200046, 200047, 200048, 200049, 200050, 200051, 200052, 200053, 200054, 200055, 200056, 200057, 200058, 200059, 200060, 200061, 200062, 200063, 200064, 200065, 200067, 200068, 200069, 200070, 200071, 200073, 200074, 200075, 200076, 200077, 200078, 200079, 200080, 200081, 200082, 200084, 200085, 200086, 200087, 200088, 200089, 200090, 200091, 200092, 200093, 200094, 200095, 200096, 200097, 200099, 200100, 200101, 200102, 200103, 200104, 200105, 200106, 200107, 200108, 200109, 200110, 200111, 200112, 200113, 200114, 200115, 200116, 200117, 200119, 200120, 200121, 200123, 200124, 200125, 200126, 200127, 200128, 200129, 200130, 200131, 200133, 200134, 200135, 200136, 200137 & 200138.

code_info

Model #: 728311; Serial #s: 200021, 200022, 200023, 200024, 200025, 200026, 200027, 200029, 200030, 200031, 200032, 200…

Model #: 728311; Serial #s: 200021, 200022, 200023, 200024, 200025, 200026, 200027, 200029, 200030, 200031, 200032, 200033, 200034, 200035, 200036, 200037, 200038, 200039, 200040, 200041, 200042, 200043, 200044, 200045, 200046, 200047, 200048, 200049, 200050, 200051, 200052, 200053, 200054, 200055, 200056, 200057, 200058, 200059, 200060, 200061, 200062, 200063, 200064, 200065, 200067, 200068, 200069, 200070, 200071, 200073, 200074, 200075, 200076, 200077, 200078, 200079, 200080, 200081, 200082, 200084, 200085, 200086, 200087, 200088, 200089, 200090, 200091, 200092, 200093, 200094, 200095, 200096, 200097, 200099, 200100, 200101, 200102, 200103, 200104, 200105, 200106, 200107, 200108, 200109, 200110, 200111, 200112, 200113, 200114, 200115, 200116, 200117, 200119, 200120, 200121, 200123, 200124, 200125, 200126, 200127, 200128, 200129, 200130, 200131, 200133, 200134, 200135, 200136, 200137 & 200138.

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-1769-2015%22

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