FDA Device recall Z-2191-2017
GE Healthcare Discovery Ml DR X-ray system
- FDA Device
- Class II
- terminated
- Published 2017-06-21
On 2017-06-21 the FDA classified a Class II recall of GE Healthcare Discovery Ml DR X-ray system by Ge Healthcare, citing it was discovered that an issue has been identified that can result in a scan starting before the prescribed delay has completed.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-2191-2017 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2017-05-19 |
| Published | 2017-06-21 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Ge Healthcare |
| Distribution | US |
Product
GE Healthcare Discovery Ml DR X-ray system
Reason
It was discovered that an issue has been identified that can result in a scan starting before the prescribed delay has completed.
Identifiers
| code_info | n/a |
|---|
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-2191-2017%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.