International safety notice
Desfibriladores-cardioversores implantables subcutáneos (S-ICD): EMBLEMTM S-ICD, modelo A209 y EMBLEMTM S-ICD MRI, modelo A219
Spain / AEMPS · ESP · Aug 26, 2019
Key facts
| Title | Desfibriladores-cardioversores implantables subcutáneos (S-ICD): EMBLEMTM S-ICD, modelo A209 y EMBLEMTM S-ICD MRI, modelo A219 |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Desfibriladores-cardioversores implantables subcutáneos (S-ICD): EMBLEMTM S-ICD, modelo A209 y EMBLEMTM S-ICD MRI, modelo A219 |
| Manufacturer | Cardiac Pacemaker Inc (Boston Scientific Corporation), EEUU |
| Models | 28042, 91.822.52.89, 92400926FA, 2019-480, 5.000.000, 92400926-FA, A209EMBLEMTM, 28022, 56.000, 20.000, 10.1016, J.HRTHM.2015.05.008 and 2 more |
| Event type | Safety Notice |
| Date | Aug 26, 2019 |
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