International safety notice
Urgent Field Safety Notice for Adapta, Versa, Sensia, Relia, Attesta, Sphera, and Vitatron A, E, G, Q series Implantable Pulse Generators (IPG) by Medtronic Inc
Germany / BfArM · DEU · Sep 23, 2019
Key facts
| Title | Urgent Field Safety Notice for Adapta, Versa, Sensia, Relia, Attesta, Sphera, and Vitatron A, E, G, Q series Implantable Pulse Generators (IPG) by Medtronic Inc |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Adapta, Versa, Sensia, Relia, Attesta, Sphera, and Vitatron A, E, G, Q series Implantable Pulse Generators (IPG) |
| Manufacturer | Medtronic Inc |
| Models | MDT2260884, 0.021, VSF21, SW010, 29901, 14-STEP, VSF20, MDT2260884-CRHF, 957DEVICES, FA857, SW043, SW003 and 1 more |
| Date | Sep 23, 2019 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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