FDA Device recall Z-1786-2015
GEMINI TF PET/CT 16 Slice (Uninterruptible Power Supply (UPS) accessory devices) Computed Tomography X-ray systems and Diagnostic Imaging s…
- FDA Device
- Class II
- terminated
- Published 2015-06-17
On 2015-06-17 the FDA classified a Class II recall of GEMINI TF PET/CT 16 Slice (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
| Agency | FDA Device |
|---|---|
| Recall number | Z-1786-2015 |
| 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
GEMINI TF PET/CT 16 Slice (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: 882456; Serial #s: 2019, 2021, 2022, 2023, 2024, 2025, 2026, 2027, 7018, 7038, 7208, 7210, 7211, 7215, 7216, 722…Model: 882456; Serial #s: 2019, 2021, 2022, 2023, 2024, 2025, 2026, 2027, 7018, 7038, 7208, 7210, 7211, 7215, 7216, 7223, 7224, 7226, 7228, 7230, 7233, 7235, 7239, 7240, 7242, 7501, 7503, 7507, 7508, 7511, 7514, 7517, 7518, 7520, 7521, 7523, 7527, 7528, 7529, 7530, 7531, 7532, 7533, 7536, 7538, 7540, 7545, 7546, 7554, 7564, 7566, 7568, 7570, 7573, 7581, 7583, 7584, 7586, 7588, 7590, 7591, 7593, 7598, 7599, 7600, 7604, 7605, 7582M & 7596M. |
|---|
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-1786-2015%22
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