International safety notice
Recall Fire Star™ and Dura Star™, Cordis
Germany / BfArM · DEU · Jan 22, 2008
Key facts
| Title | Recall Fire Star™ and Dura Star™, Cordis |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall Fire Star™ and Dura Star™, Cordis |
| Manufacturer | Recall Fire Star™ and Dura Star™, Cordis |
| Models | 8012015$, 0120400, 0125225, 70125350, 70130325, 70130300, 70125400, 70125375, 80115225, 80110275, 3315455, 10250 and 72 more |
| Date | Jan 22, 2008 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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