International safety notice
Lot Recall for the S.M.A.R.T. ® Nitinol Stent System and S.M.A.R.T. ® CONTROL ® Nitinol Stent System, Cordis
Germany / BfArM · DEU · Aug 22, 2012
Key facts
| Title | Lot Recall for the S.M.A.R.T. ® Nitinol Stent System and S.M.A.R.T. ® CONTROL ® Nitinol Stent System, Cordis |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the S.M.A.R.T. ® Nitinol Stent System and S.M.A.R.T. ® CONTROL ® Nitinol Stent System, Cordis |
| Manufacturer | Lot Recall for the S.M.A.R.T. ® Nitinol Stent System and S.M.A.R.T. ® CONTROL ® Nitinol Stent System, Cordis |
| Models | 2014-01, C06120MV, C06150SV, 15565254, C07040SV, 15561454, C10060SV, 15562691, 15567995, C07150MV, 15540281, 15539561 and 40 more |
| Date | Aug 22, 2012 |
| 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