International safety notice
Recall for Ultraflex Esophageal™ NG Stent System; Ultraflex™ Tracheobronchial Stent System and Ultraflex™ Precision Colonic Stent System, Boston Scientific
Germany / BfArM · DEU · Aug 17, 2010
Key facts
| Title | Recall for Ultraflex Esophageal™ NG Stent System; Ultraflex™ Tracheobronchial Stent System and Ultraflex™ Precision Colonic Stent System, Boston Scientific |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Ultraflex Esophageal™ NG Stent System; Ultraflex™ Tracheobronchial Stent System and Ultraflex™ Precision Colonic Stent System, Boston Scientific |
| Manufacturer | Recall for Ultraflex Esophageal™ NG Stent System; Ultraflex™ Tracheobronchial Stent System and Ultraflex™ Precision Colonic Stent System, Boston Scientific |
| Models | 13453530, 13436212, M00564670, M00513860, M00513720, 13432574, M00514200, M00564860, M00513740, 13435072, 13439023, 13441743 and 22 more |
| Date | Aug 17, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models 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