International safety notice
Corrective action of the m2000sp und m1000 analyzers from Abbott
Germany / BfArM · DEU · Jul 12, 2007
Key facts
| Title | Corrective action of the m2000sp und m1000 analyzers from Abbott |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Corrective action of the m2000sp und m1000 analyzers from Abbott |
| Manufacturer | Corrective action of the m2000sp und m1000 analyzers from Abbott |
| Models | M2000SPTM, 9K14-01, 4J72-01, 60018-3315, FA-CAM-JUN2007-015, M2000SP |
| Date | Jul 12, 2007 |
| 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