FDA Device recall Z-1765-2015

Brilliance CT 16 Slice Air (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging…

FDA Device
Class II
terminated
Published 2015-06-17

On 2015-06-17 the FDA classified a Class II recall of Brilliance CT 16 Slice Air (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging… 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-1765-2015
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 16 Slice Air (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 #: 728246; Serial #s: 3007, 3011, 3014, 3047, 3050, 3095, 3117, 3123, 3162, 3164, 3170, 3197, 3247, 3331, 3407, 3… Model #: 728246; Serial #s: 3007, 3011, 3014, 3047, 3050, 3095, 3117, 3123, 3162, 3164, 3170, 3197, 3247, 3331, 3407, 3433, 3458, 3497, 3578, 3721, 3723, 4015, 4019, 4042, 5013, 5019, 5038, 5040, 5050, 5052, 5090, 5091, 5094, 5097, 5101, 5116, 5133, 5143, 5150, 5155, 5172, 5179, 5180, 5192, 5202, 5252, 5335, 5336, 5342, 5343, 5399, 5416, 5455, 5467, 5601, 5703, 5811, 5869, 5929, 6006, 6012, 6021, 6030, 6037, 6038, 6039, 6043, 6045, 6048, 6051, 6055, 6056, 6064, 6071, 6072, 6074, 6076, 6078, 6079, 6081, 6082, 6083, 6084, 6085, 6087, 6088, 6089, 6090, 6092, 6093, 6094, 6095, 6097, 6100, 6104, 6105, 6107, 6109, 6110, 6111, 6112, 6114, 6116, 6118, 6119, 6120, 6122, 6123, 6124, 6125, 6126, 6127, 6128, 6129, 6130, 6131, 6132, 6133, 6135, 6136, 6137, 6139, 6140, 6141, 6143, 6144, 6145, 6146, 6147, 6148, 6149, 6151, 6153, 6155, 6156, 6157, 6159, 6161, 6162, 6163, 6164, 6165, 6166, 6167, 6168, 6169, 6170, 6171, 6172, 6173, 6174, 6175, 6176, 6177, 6178, 6179, 6180, 6181, 6182, 6183, 6184, 6185,

code_info

Model #: 728246; Serial #s: 3007, 3011, 3014, 3047, 3050, 3095, 3117, 3123, 3162, 3164, 3170, 3197, 3247, 3331, 3407, 3…

Model #: 728246; Serial #s: 3007, 3011, 3014, 3047, 3050, 3095, 3117, 3123, 3162, 3164, 3170, 3197, 3247, 3331, 3407, 3433, 3458, 3497, 3578, 3721, 3723, 4015, 4019, 4042, 5013, 5019, 5038, 5040, 5050, 5052, 5090, 5091, 5094, 5097, 5101, 5116, 5133, 5143, 5150, 5155, 5172, 5179, 5180, 5192, 5202, 5252, 5335, 5336, 5342, 5343, 5399, 5416, 5455, 5467, 5601, 5703, 5811, 5869, 5929, 6006, 6012, 6021, 6030, 6037, 6038, 6039, 6043, 6045, 6048, 6051, 6055, 6056, 6064, 6071, 6072, 6074, 6076, 6078, 6079, 6081, 6082, 6083, 6084, 6085, 6087, 6088, 6089, 6090, 6092, 6093, 6094, 6095, 6097, 6100, 6104, 6105, 6107, 6109, 6110, 6111, 6112, 6114, 6116, 6118, 6119, 6120, 6122, 6123, 6124, 6125, 6126, 6127, 6128, 6129, 6130, 6131, 6132, 6133, 6135, 6136, 6137, 6139, 6140, 6141, 6143, 6144, 6145, 6146, 6147, 6148, 6149, 6151, 6153, 6155, 6156, 6157, 6159, 6161, 6162, 6163, 6164, 6165, 6166, 6167, 6168, 6169, 6170, 6171, 6172, 6173, 6174, 6175, 6176, 6177, 6178, 6179, 6180, 6181, 6182, 6183, 6184, 6185,

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-1765-2015%22

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