International safety notice
Recall for the ThruPort™ Knot Pusher Model KP1 and Valve Placement Pack Model VPP, Edwards Lifesciences LLC
Germany / BfArM · DEU · Sep 16, 2015
Key facts
| Title | Recall for the ThruPort™ Knot Pusher Model KP1 and Valve Placement Pack Model VPP, Edwards Lifesciences LLC |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the ThruPort™ Knot Pusher Model KP1 and Valve Placement Pack Model VPP, Edwards Lifesciences LLC |
| Manufacturer | Recall for the ThruPort™ Knot Pusher Model KP1 and Valve Placement Pack Model VPP, Edwards Lifesciences LLC |
| Models | 60089865, «ADD_1», 60045802, 60016312, 60066591, FCA-69, 60045801, 59964698, 60059982, 60022521, 59984375, 60022522 and 3 more |
| Date | Sep 16, 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