International safety notice
Recall for RF Ablation System Foot-Switch, Boston Scientific
Germany / BfArM · DEU · Jul 30, 2009
Key facts
| Title | Recall for RF Ablation System Foot-Switch, Boston Scientific |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | RF Ablation System Foot-Switch, Boston Scientific |
| Manufacturer | Recall for RF Ablation System Foot-Switch, Boston Scientific |
| Models | 91248, 91510, 62902, 64243, 94434, 56805, 63316, 91521, 91516, 020199-007, 63349, 2973046 and 1292 more |
| Date | Jul 30, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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