International safety notice
General names: (1) Extractor-type SPECT device for nuclear medicine diagnosis (2) X-ray CT combined type SPECT device Brand name: (1) Nuclear medicine diagnostic device Discovery NM 630 (2) Nuclear medicine diagnostic device Discovery NM/CT 670
Japan / PMDA Recalls · JPN · Dec 21, 2022
Key facts
| Regulator | Japan / PMDA Recalls |
|---|---|
| Country | JPN |
| Brand | General names: (1) Extractor-type SPECT device for nuclear medicine diagnosis (2) X-ray CT combined type SPECT device Brand name: (1) Nuclear medicine diagnostic device Discovery NM 630 (2) Nuclear medicine diagnostic device Discovery NM/CT 670 |
| Manufacturer | GE Healthcare Japan Co., Ltd. |
| Models | NS0208, NS0549, NM0038, NT3112, NM0044, NS0526, NS0536, NS0202, NS0544, NS0566, NS0525, NS0205 and 111 more |
| Date | Dec 21, 2022 |
| Regulator page | info.pmda.go.jp |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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