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FDA Device recall Z-1762-2015

Brilliance CT 40 - Slices (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging s…

On 2015-06-17 the FDA classified a Class II recall of Brilliance CT 40 - Slices (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging s… 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

AgencyFDA Device
Recall numberZ-1762-2015
ClassificationClass II
Statusterminated
Initiated2015-03-06
Published2015-06-17
Last updated2026-09-13 11:53 UTC
CompanyPhilips Medical Systems Cleveland
DistributionUS

Product

Brilliance CT 40 - Slices (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_infoModel #: 728235; Serial #s: 9266, 9267, 9268, 9269, 9271, 9272, 9273, 9275, 9276, 9277, 9278, 9280, 9281, 9282, 9284, 9285 & 9286.

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-1762-2015%22

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