FDA Device recall Z-1761-2015

Brilliance CT 64 channel with Essence, Technology (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems…

FDA Device
Class II
terminated
Published 2015-06-17

On 2015-06-17 the FDA classified a Class II recall of Brilliance CT 64 channel with Essence, Technology (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray 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-1761-2015
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

Brilliance CT 64 channel with Essence, Technology (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 #: 728231; Serial #s: 7521, 7546, 9038, 9043, 9044, 9047, 9050, 9072, 9106, 9120, 9152, 9168, 9234, 9250, 9516, 9… Model #: 728231; Serial #s: 7521, 7546, 9038, 9043, 9044, 9047, 9050, 9072, 9106, 9120, 9152, 9168, 9234, 9250, 9516, 9526, 9535, 9551, 9552, 9564, 9604, 9627, 9641, 9654, 9655, 9663, 9664, 9690, 9701, 9763, 9782, 9870, 9915, 9982, 9996, 10066, 10067, 10188, 10201, 10213, 10216, 10218, 10221, 10222, 10223, 10225, 10226, 10227, 10229, 10235, 10237, 10242, 10245, 10248, 10250, 10251, 10253, 10254, 10256, 10257, 10258, 10259, 10261, 10263, 10265, 10266, 10267, 10269, 10270, 10271, 10274, 10275, 10276, 10277, 10278, 10279, 10280, 10281, 10282, 10283, 10284, 10285, 10286, 10287, 10288, 10291, 10292, 10293, 10294, 10295, 10296, 10297, 10298, 10299, 10300, 10301, 10302, 10303, 10304, 10305, 10307, 10308, 10309, 10310, 10311, 10312, 10313, 10314, 10315, 10316, 10317, 10318, 10319, 10320, 10321, 10322, 10323, 10324, 10325, 10327, 10330, 10331, 10332, 10333, 10334, 10335, 10336, 10337, 10338, 10339, 10341, 10342, 10343, 10344, 10345, 10346, 10347, 10348, 10349, 10350, 10351, 10352, 10353, 10354,

code_info

Model #: 728231; Serial #s: 7521, 7546, 9038, 9043, 9044, 9047, 9050, 9072, 9106, 9120, 9152, 9168, 9234, 9250, 9516, 9…

Model #: 728231; Serial #s: 7521, 7546, 9038, 9043, 9044, 9047, 9050, 9072, 9106, 9120, 9152, 9168, 9234, 9250, 9516, 9526, 9535, 9551, 9552, 9564, 9604, 9627, 9641, 9654, 9655, 9663, 9664, 9690, 9701, 9763, 9782, 9870, 9915, 9982, 9996, 10066, 10067, 10188, 10201, 10213, 10216, 10218, 10221, 10222, 10223, 10225, 10226, 10227, 10229, 10235, 10237, 10242, 10245, 10248, 10250, 10251, 10253, 10254, 10256, 10257, 10258, 10259, 10261, 10263, 10265, 10266, 10267, 10269, 10270, 10271, 10274, 10275, 10276, 10277, 10278, 10279, 10280, 10281, 10282, 10283, 10284, 10285, 10286, 10287, 10288, 10291, 10292, 10293, 10294, 10295, 10296, 10297, 10298, 10299, 10300, 10301, 10302, 10303, 10304, 10305, 10307, 10308, 10309, 10310, 10311, 10312, 10313, 10314, 10315, 10316, 10317, 10318, 10319, 10320, 10321, 10322, 10323, 10324, 10325, 10327, 10330, 10331, 10332, 10333, 10334, 10335, 10336, 10337, 10338, 10339, 10341, 10342, 10343, 10344, 10345, 10346, 10347, 10348, 10349, 10350, 10351, 10352, 10353, 10354,

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-1761-2015%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.