International safety notice
Urgent Field Safety Notice for KYPHON Express Directional Bone Filler by Medtronic Sofamor Danek Inc.
Germany / BfArM · DEU · Dec 15, 2017
Key facts
| Title | Urgent Field Safety Notice for KYPHON Express Directional Bone Filler by Medtronic Sofamor Danek Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | KYPHON Express Directional Bone Filler |
| Manufacturer | Medtronic Sofamor Danek Inc. |
| Models | WI439940, WI428822, WI449819, WI455595, WI459477, WI463434, WI472178, WI472177, WI446722, FA793, WI472176, WI435227 and 4 more |
| Date | Dec 15, 2017 |
| 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