International safety notice
Sistemas de medicina nuclear: • Discovery NM 630 • Discovery NM/CT 670 DR • Discovery NM/CT 670 Pro • NM 830 • NM/CT 850 • NM/CT 850 ES • NM/CT 860 • NM/CT 870 CZT • NM/CT 870 DR fabricados entre mayo y diciembre de 2018.
Spain / AEMPS · ESP · Sep 14, 2020
Key facts
| Title | Sistemas de medicina nuclear: • Discovery NM 630 • Discovery NM/CT 670 DR • Discovery NM/CT 670 Pro • NM 830 • NM/CT 850 • NM/CT 850 ES • NM/CT 860 • NM/CT 870 CZT • NM/CT 870 DR fabricados entre mayo y diciembre de 2018. |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Sistemas de medicina nuclear: • Discovery NM 630 • Discovery NM/CT 670 DR • Discovery NM/CT 670 Pro • NM 830 • NM/CT 850 • NM/CT 850 ES • NM/CT 860 • NM/CT 870 CZT • NM/CT 870 DR fabricados entre mayo y diciembre de 2018. |
| Manufacturer | GE Medical Systems Israel, Functional Imaging, Israel. |
| Models | 35-37, 28023, 53188, 40890, 61919, 28022, 2020-521, FMI40890_FSN_SPANISH_REV6, 91.822.52.89 |
| Event type | Safety Notice |
| Date | Sep 14, 2020 |
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