International safety notice
Recall of the E-vita THORACIC 3G Stent Graft System, Jotec GmbH
Germany / BfArM · DEU · Dec 5, 2013
Key facts
| Title | Recall of the E-vita THORACIC 3G Stent Graft System, Jotec GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the E-vita THORACIC 3G Stent Graft System, Jotec GmbH |
| Manufacturer | Recall of the E-vita THORACIC 3G Stent Graft System, Jotec GmbH |
| Models | 07471, 72379, 922-0, 420851, 922-100 |
| Date | Dec 5, 2013 |
| 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