International safety notice
GE Healthcare
United Kingdom / MHRA · GBR · Sep 27, 2021
Key facts
| Title | GE Healthcare |
|---|---|
| Regulator | United Kingdom / MHRA |
| Country | GBR |
| Brand | SIGNA Premier RX29.1 SIGNA Architect DV29.1 SIGNA Pioneer PX29.1 Discovery MR750 3.0T, Discovery MR750w 3.0T DV29.1 Optima MR450w 1.5T DV29.1 |
| Manufacturer | GE Healthcare |
| Models | 53188, PX26.4, 00840682145770, 00195278126443, PX25.4, PX29.1, DV28.4, 00195278229519, 00840682147095, HD29.1, DV29.1, 00195278416339 and 34 more |
| Event type | Recall, Safety Notice |
| Action type | Field safety notice |
| Date | Sep 27, 2021 |
| Regulator page | gov.uk |
At a glance
- Yes 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