FDA Device recall Z-2737-2016
BrightView XCT Upgrade Model 882454
- FDA Device
- Class II
- terminated
- Published 2016-09-14
On 2016-09-14 the FDA classified a Class II recall of BrightView XCT Upgrade Model 882454 by Philips Medical Systems Cleveland, citing the firm became aware of an issue where during a non-Auto Body Contouring (ABC), non-circular, rel-180 scan, the detector may come in contact with the patient. The issue was cause….
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2737-2016 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2016-05-25 |
| Published | 2016-09-14 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Philips Medical Systems Cleveland |
| Distribution | US |
Product
BrightView XCT Upgrade Model 882454
Reason
The firm became aware of an issue where during a non-Auto Body Contouring (ABC), non-circular, rel-180 scan, the detector may come in contact with the patient. The issue was caused by a software defect in the workflow setup script.
Identifiers
| code_info | 11000021, 11000082, 11000111 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-2737-2016%22
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