International safety notice
Recall of the wheelchairs Invacare Action², Invacare/Aquatec
Germany / BfArM · DEU · Dec 13, 2007
Key facts
| Title | Recall of the wheelchairs Invacare Action², Invacare/Aquatec |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the wheelchairs Invacare Action², Invacare/Aquatec |
| Manufacturer | Recall of the wheelchairs Invacare Action², Invacare/Aquatec |
| Models | ACTION2, 88305, 0084005, 3446763, 621088, 54-52, 1504140, «NAME3»«NAME4», 197309689, 1504139, »«NAME2», 036200 and 8 more |
| Date | Dec 13, 2007 |
| 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