International safety notice
Recall of all “Action 2000” manual wheelchairs of manufacturer Invacare Aquatec GmbH
Germany / BfArM · DEU · Jul 2, 2009
Key facts
| Title | Recall of all “Action 2000” manual wheelchairs of manufacturer Invacare Aquatec GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of all “Action 2000” manual wheelchairs of manufacturer Invacare Aquatec GmbH |
| Manufacturer | Recall of all “Action 2000” manual wheelchairs of manufacturer Invacare Aquatec GmbH |
| Models | ACTION02, 7008568013, 7007533957, 88316 |
| Date | Jul 2, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No 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