FDA Device recall Z-1755-2019
Silhouette VR This fully integrated system offers intuitive controls with advanced applications for maximum performance all in a space-savi…
- FDA Device
- Class II
- terminated
- Published 2019-06-19
On 2019-06-19 the FDA classified a Class II recall of Silhouette VR This fully integrated system offers intuitive controls with advanced applications for maximum performance all in a space-savi… by Ge Healthcare, citing there has been a reported incident of a Distar CRT monitor that has fallen off the monitor wall mount related to product aging.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-1755-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-03-29 |
| Published | 2019-06-19 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
Silhouette VR This fully integrated system offers intuitive controls with advanced applications for maximum performance all in a space-saving design.
Reason
There has been a reported incident of a Distar CRT monitor that has fallen off the monitor wall mount related to product aging.
Identifiers
| code_info | DZ1061RX02 and UP389014. |
|---|
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-1755-2019%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.