International safety notice
MyoSPECT (fabricado el 13-02-2024 o con anterioridad); MyoSPECT ES (fabricado el 15-02-2024 o con anterioridad)
Spain / AEMPS · ESP · May 9, 2024
Key facts
| Title | MyoSPECT (fabricado el 13-02-2024 o con anterioridad); MyoSPECT ES (fabricado el 15-02-2024 o con anterioridad) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | MyoSPECT (fabricado el 13-02-2024 o con anterioridad); MyoSPECT ES (fabricado el 15-02-2024 o con anterioridad) |
| Manufacturer | GE Medical Systems, Israel |
| Models | RECALL.40906, 91.822.52.89, 40906, 105776, 00195278421579, 1302-2024, 00195278421586, 15-02-2024, 13-02-2024, 28023, 00195278488619, 28022 and 3 more |
| Event type | Safety Notice |
| Date | May 9, 2024 |
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