International safety notice
Recall of Endurant / Endurant II 23 mm and 25 mm Bifurcated Stent Graft Systems, Medtronic
Germany / BfArM · DEU · Mar 2, 2017
Key facts
| Title | Recall of Endurant / Endurant II 23 mm and 25 mm Bifurcated Stent Graft Systems, Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of Endurant / Endurant II 23 mm and 25 mm Bifurcated Stent Graft Systems, Medtronic |
| Manufacturer | Recall of Endurant / Endurant II 23 mm and 25 mm Bifurcated Stent Graft Systems, Medtronic |
| Models | ENBF2513C170EE, ETBF2516C124EE, ETBF2316C145EE, ETBF2516C145EE, ETBF2513C166EE, ETBF2316C166EE, ENBF2316C170EE, ENBF2313C170EE, ENBF2516C170EE, ETBF2516C145E, ETBF2313C124EE, ENBF2313C120EE and 15 more |
| Date | Mar 2, 2017 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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