RecallRadar

FDA Device recall Z-1778-2015

Precedence 16 (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging systems

On 2015-06-17 the FDA classified a Class II recall of Precedence 16 (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

AgencyFDA Device
Recall numberZ-1778-2015
ClassificationClass II
Statusterminated
Initiated2015-03-06
Published2015-06-17
Last updated2026-09-13 11:53 UTC
CompanyPhilips Medical Systems Cleveland
DistributionUS

Product

Precedence 16 (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 #: 882350; Serial #s: 300072, 3000068, 3000071, 3000073, 3000074, 3000075, 3000076, 3000077, 3000078, 3000079, 30…Model #: 882350; Serial #s: 300072, 3000068, 3000071, 3000073, 3000074, 3000075, 3000076, 3000077, 3000078, 3000079, 3000081, 3000082, 3000083, 3000084, 3000085, 3000086, 3000087, 3000088, 3000089, 3000090, 3000091, 3000092, 3000093, 3000094, 3000095, 3000096, 3000097, 3000098, 3000099, 3000100, 3000101, 3000102, 3000103, 3000104, 3000105 & 3000106.

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-1778-2015%22

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