International safety notice
Sistemas de resonancia magnética móviles con Twinspeed: GE Signa 1.5T TwinSpeed, 1.5T Signa Excite HD, 3.0T Signa Excite HD, GE Signa 3.0T con Excite, GE 1.5T Signa HDx, 3.0T Signa HDx, GE 1.5T HDxt, GE 3.0T Signa HDxt, 1.5T Signa HDxt.
Spain / AEMPS · ESP · Mar 16, 2022
Key facts
| Title | Sistemas de resonancia magnética móviles con Twinspeed: GE Signa 1.5T TwinSpeed, 1.5T Signa Excite HD, 3.0T Signa Excite HD, GE Signa 3.0T con Excite, GE 1.5T Signa HDx, 3.0T Signa HDx, GE 1.5T HDxt, GE 3.0T Signa HDxt, 1.5T Signa HDxt. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistemas de resonancia magnética móviles con Twinspeed: GE Signa 1.5T TwinSpeed, 1.5T Signa Excite HD, 3.0T Signa Excite HD, GE Signa 3.0T con Excite, GE 1.5T Signa HDx, 3.0T Signa HDx, GE 1.5T HDxt, GE 3.0T Signa HDxt, 1.5T Signa HDxt. |
| Manufacturer | GE Medical Systems, LLC, EEUU. |
| Models | 2022-130, 35-37, 53188, 91.822.52.89, 78015, RECALL.60984, 60984, 2022PUEDE, 28022, 28023 |
| Event type | Safety Notice |
| Date | Mar 16, 2022 |
At a glance
- No Recall
- Yes Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers in FDA data
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About International device safety notices
Field safety notices, recalls and safety alerts published by about 30 national medical device regulators outside the United States, matched by Orca1 to FDA device data.
Source: National medical device regulators (as listed), compiled by Orca1