FDA Device recall Z-1923-2020
Philips Brilliance IQon Spectral CT, Computed Tomography X-Ray System
- FDA Device
- Class II
- terminated
- Published 2020-05-13
On 2020-05-13 the FDA classified a Class II recall of Philips Brilliance IQon Spectral CT, Computed Tomography X-Ray System by Philips North America, citing the bolt affixing the cooling unit to the rotor was not tightened to specification on the Philips Brilliance iCT systems.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1923-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2020-04-06 |
| Published | 2020-05-13 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Philips North America |
| Distribution | IA |
Product
Philips Brilliance IQon Spectral CT, Computed Tomography X-Ray System; Model # 728332; UDI # (01)00884838059542(21)860067
Reason
The bolt affixing the cooling unit to the rotor was not tightened to specification on the Philips Brilliance iCT systems.
Identifiers
| code_info | Serial #s 860067, 860023 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1923-2020%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.