International safety notice
Otto Bock recalled the powered wheelchairs C1000 and B600
Germany / BfArM · DEU · Dec 2, 2005
Key facts
| Title | Otto Bock recalled the powered wheelchairs C1000 and B600 |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Otto Bock recalled the powered wheelchairs C1000 and B600 |
| Manufacturer | Otto Bock recalled the powered wheelchairs C1000 and B600 |
| Models | 493U32=SK130, 37115, C1000 |
| Date | Dec 2, 2005 |
| 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