International safety notice
Problems with the Bloom Programmable Stimulator from Fisher Imaging
Germany / BfArM · DEU · Jul 29, 2005
Key facts
| Title | Problems with the Bloom Programmable Stimulator from Fisher Imaging |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Problems with the Bloom Programmable Stimulator from Fisher Imaging |
| Manufacturer | Problems with the Bloom Programmable Stimulator from Fisher Imaging |
| Models | 12300, 800-448-4793, 80241 |
| Date | Jul 29, 2005 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers 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