FDA Device recall Z-1784-2015

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

FDA Device
Class II
terminated
Published 2015-06-17

On 2015-06-17 the FDA classified a Class II recall of CardioMD III (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

Agency	FDA Device
Recall number	Z-1784-2015
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

CardioMD III (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 #: 882450; Serial #s: 1106080, 1122002, 2112702, 3101001, 4042003, 4112402, 5032201, 5032902, 5042501, 5060701, 6… Model #: 882450; Serial #s: 1106080, 1122002, 2112702, 3101001, 4042003, 4112402, 5032201, 5032902, 5042501, 5060701, 6030802, 7092001, 9042902, 9053001, 9061602, 9070702, 9081002, 9083101, 9083102, 9090301, 9090302, 9091101, 9092201, 9092202, 9101302, 9101901, 9102302, 9102801, 9102802, 9111601, 9111602, 9120902, 10020201, 10062906, 10071301, 10090201, 10090202, 10100501, 10100502, 10100701, 10100702, 10110303, 10110801, 10110802, 10120901, 10120902, 10121001, 10121002, 11021601, 11021602, 11031001, 11031002, 11041201, 11041202, 11051101, 11051102, 11070401, 11070402, 11072102, 11090801, 11090802, 11112301, 11120501, 11120502, 11121201, 11121202, 11121402, 12010601, 12012702, 12020101, 12020102, 12041201, 12052201, 12053001, 12053002, 12071101, 12071102, 12071201, 12071401, 110110804 & 110110806.

code_info

Model #: 882450; Serial #s: 1106080, 1122002, 2112702, 3101001, 4042003, 4112402, 5032201, 5032902, 5042501, 5060701, 6…

Model #: 882450; Serial #s: 1106080, 1122002, 2112702, 3101001, 4042003, 4112402, 5032201, 5032902, 5042501, 5060701, 6030802, 7092001, 9042902, 9053001, 9061602, 9070702, 9081002, 9083101, 9083102, 9090301, 9090302, 9091101, 9092201, 9092202, 9101302, 9101901, 9102302, 9102801, 9102802, 9111601, 9111602, 9120902, 10020201, 10062906, 10071301, 10090201, 10090202, 10100501, 10100502, 10100701, 10100702, 10110303, 10110801, 10110802, 10120901, 10120902, 10121001, 10121002, 11021601, 11021602, 11031001, 11031002, 11041201, 11041202, 11051101, 11051102, 11070401, 11070402, 11072102, 11090801, 11090802, 11112301, 11120501, 11120502, 11121201, 11121202, 11121402, 12010601, 12012702, 12020101, 12020102, 12041201, 12052201, 12053001, 12053002, 12071101, 12071102, 12071201, 12071401, 110110804 & 110110806.

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-1784-2015%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.