International safety notice
Recall / Corrective Action for m2000sp Instrument, Abbott
Germany / BfArM · DEU · Sep 17, 2008
Key facts
| Title | Recall / Corrective Action for m2000sp Instrument, Abbott |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | m2000sp Instrument, Abbott |
| Manufacturer | Recall / Corrective Action for m2000sp Instrument, Abbott |
| Models | 9K14-02, M2000SPTM, FA-CAM-JUN20W025V2, M2000SP, 60018-3315, 9K14-OI |
| Date | Sep 17, 2008 |
| 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