International safety notice
Recall for the Coroflex Isar Coronary stent, B. Braun Melsungen AG, Division Aesculap Vascular Systems
Germany / BfArM · DEU · Jun 3, 2015
Key facts
| Title | Recall for the Coroflex Isar Coronary stent, B. Braun Melsungen AG, Division Aesculap Vascular Systems |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Coroflex Isar Coronary stent, B. Braun Melsungen AG, Division Aesculap Vascular Systems |
| Manufacturer | Recall for the Coroflex Isar Coronary stent, B. Braun Melsungen AG, Division Aesculap Vascular Systems |
| Models | 12359, 5A20809, 568207-170, 502871, 568207-123 |
| Date | Jun 3, 2015 |
| 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