International safety notice
Recall for Ablation System Foot Switch, Boston Scientific Corp.
Germany / BfArM · DEU · Dec 22, 2008
Key facts
| Title | Recall for Ablation System Foot Switch, Boston Scientific Corp. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Ablation System Foot Switch, Boston Scientific Corp. |
| Manufacturer | Recall for Ablation System Foot Switch, Boston Scientific Corp. |
| Models | 053이00051, 0629900283, 0610000091, 0606100079, 062370이61, 0629900222, 0610000104, 0626500203, 062650이87, 0629900304, 062020이32, 0620200109 and 396 more |
| Date | Dec 22, 2008 |
| 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