International safety notice
Field Safety Notice concerning corrective actions on Explorer and Discovery X-ray Bone Densitometer Systems, Hologic
Germany / BfArM · DEU · Jun 26, 2009
Key facts
| Title | Field Safety Notice concerning corrective actions on Explorer and Discovery X-ray Bone Densitometer Systems, Hologic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Field Safety Notice concerning corrective actions on Explorer and Discovery X-ray Bone Densitometer Systems, Hologic |
| Manufacturer | Field Safety Notice concerning corrective actions on Explorer and Discovery X-ray Bone Densitometer Systems, Hologic |
| Models | 1.781, 1.781.999.7300, 32.2.71, 140-0090, 1.781280.0669, 32.2.711, 280.0669, 01730 |
| Date | Jun 26, 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