International safety notice
Marcapasos implantables bicamerales: Adapta™, Versa™, Sensia™, Relia™, Attesta™, Sphera™, y Vitatron™ series A, E, G, Q. (Distribuidos entre el 10 de marzo de 2017 y el 7 de enero de 2019)
Spain / AEMPS · ESP · Feb 1, 2019
Key facts
| Title | Marcapasos implantables bicamerales: Adapta™, Versa™, Sensia™, Relia™, Attesta™, Sphera™, y Vitatron™ series A, E, G, Q. (Distribuidos entre el 10 de marzo de 2017 y el 7 de enero de 2019) |
|---|---|
| Regulator | Spain / AEMPS |
| Country | ESP |
| Brand | Marcapasos implantables bicamerales: Adapta™, Versa™, Sensia™, Relia™, Attesta™, Sphera™, y Vitatron™ series A, E, G, Q. (Distribuidos entre el 10 de marzo de 2017 y el 7 de enero de 2019) |
| Manufacturer | Medtronic INC,EEUU |
| Models | 49933, 28050, MDT2260884-CRHF, ALERTA2019-059, 2019-059, 91.822.52.89, MDT2260884, FA857, 28022 |
| Event type | Safety Notice |
| Date | Feb 1, 2019 |
At a glance
- No Recall
- Yes Field safety notice
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