International safety notice
Medtronic recalls the DLP VAD Cannula for Ventricular Assist and the Cardio Kits C390601A, C391102A, M850313A
Germany / BfArM · DEU · Dec 21, 2004
Key facts
| Title | Medtronic recalls the DLP VAD Cannula for Ventricular Assist and the Cardio Kits C390601A, C391102A, M850313A |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Ventricular Assist and the Cardio Kits C390601A, C391102A, M850313A |
| Manufacturer | Medtronic recalls the DLP VAD Cannula for Ventricular Assist and the Cardio Kits C390601A, C391102A, M850313A |
| Models | 06112, 2003090147, 5293-109, 5293-106, C391102A, 58081-22, 590510939, 40547, 356013, C390601A, 5293-0, M850313A and 14 more |
| Date | Dec 21, 2004 |
| 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