International safety notice
Recall for the EOPA® Arterial Cannula, Medtronic
Germany / BfArM · DEU · Aug 10, 2015
Key facts
| Title | Recall for the EOPA® Arterial Cannula, Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the EOPA® Arterial Cannula, Medtronic |
| Manufacturer | Recall for the EOPA® Arterial Cannula, Medtronic |
| Models | 14512600, FA673, 0.038”, 2015060544, 77620 |
| Date | Aug 10, 2015 |
| 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