International safety notice
Recall of the Select 3D™ and Select CAP™ Arterial Cannula product families, Medtronic
Germany / BfArM · DEU · Feb 11, 2014
Key facts
| Title | Recall of the Select 3D™ and Select CAP™ Arterial Cannula product families, Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the Select 3D™ and Select CAP™ Arterial Cannula product families, Medtronic |
| Manufacturer | Recall of the Select 3D™ and Select CAP™ Arterial Cannula product families, Medtronic |
| Models | 78722, 78922, 78920, CB78722, 78622, 78724, 78924, FA604, 78624, C300901B, 78618, 78820 and 6 more |
| Date | Feb 11, 2014 |
| 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