International safety notice
Recall of implantable pulse generators for neurostimulation EON MINI and BRIO, St. Jude Medical
Germany / BfArM · DEU · May 31, 2011
Key facts
| Title | Recall of implantable pulse generators for neurostimulation EON MINI and BRIO, St. Jude Medical |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | neurostimulation EON MINI and BRIO, St. Jude Medical |
| Manufacturer | Recall of implantable pulse generators for neurostimulation EON MINI and BRIO, St. Jude Medical |
| Models | 705754, 13757944, 711903, 13501593, 13556282, 13763305, 13765995, 709155, 710416, 710735, 13765885, 13758839 and 1639 more |
| Date | May 31, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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