International safety notice
Recall of S.M.A.R.T. Flex Vascular Stent System, Cordis Corporation
Germany / BfArM · DEU · Mar 24, 2017
Key facts
| Title | Recall of S.M.A.R.T. Flex Vascular Stent System, Cordis Corporation |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of S.M.A.R.T. Flex Vascular Stent System, Cordis Corporation |
| Manufacturer | Recall of S.M.A.R.T. Flex Vascular Stent System, Cordis Corporation |
| Models | 37350, 35756, 34589, 20705032066829, SF05200MV, 36792, 36865, 37168, 34551, 38320, 39974, 2018-11-22 and 147 more |
| Date | Mar 24, 2017 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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