International safety notice
Recall of the MAV™ instruments of Medtronic
Germany / BfArM · DEU · May 24, 2006
Key facts
| Title | Recall of the MAV™ instruments of Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the MAV™ instruments of Medtronic |
| Manufacturer | Recall of the MAV™ instruments of Medtronic |
| Models | M04H0009, IM05KIOO, IM05C159, M04K03351, IM05C158, 8995401, IM05C157, 8995403, IM05K087, M04HK00631, IM05G080, DC05H004A and 32 more |
| Date | May 24, 2006 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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