International safety notice
Recall of the DLP® Femoral Arterial Cannula product and DLP® Femoral Cannula and Insertion Kits, Medtronic
Germany / BfArM · DEU · Jun 16, 2015
Key facts
| Title | Recall of the DLP® Femoral Arterial Cannula product and DLP® Femoral Cannula and Insertion Kits, Medtronic |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the DLP® Femoral Arterial Cannula product and DLP® Femoral Cannula and Insertion Kits, Medtronic |
| Manufacturer | Recall of the DLP® Femoral Arterial Cannula product and DLP® Femoral Cannula and Insertion Kits, Medtronic |
| Models | 201503C101, 2015021260, 2015016695, 2015016410, 2015021484, 2015021134, 2015016317, 2015030629, 2015020566, 2015020381, 57417, 201501C886 and 15 more |
| Date | Jun 16, 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