RecallRadar

FDA Device recall Z-1766-2015

Brilliance CT 6 Slice Air (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 6 Slice Air (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-1766-2015
ClassificationClass II
Statusterminated
Initiated2015-03-06
Published2015-06-17
Last updated2026-09-13 11:53 UTC
CompanyPhilips Medical Systems Cleveland
DistributionUS

Product

Brilliance CT 6 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 #: 728256; Serial #s: 3683, 3687, 3691, 3692, 3693, 3695, 3696, 3703, 3704, 3705, 3706, 3707, 3708, 3709, 3710, 3…Model #: 728256; Serial #s: 3683, 3687, 3691, 3692, 3693, 3695, 3696, 3703, 3704, 3705, 3706, 3707, 3708, 3709, 3710, 3711, 3712, 3713, 3714, 3715, 3717, 3718, 3719, 3720 & 3722

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-1766-2015%22

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