International safety notice
Urgent field safety notice for instruments and containers: Java pedicle screw system / Fidji cervical / lumbar cage / Wallis posterior dynamic stabilization system, Zimmer Biomet
Germany / BfArM · DEU · Dec 16, 2016
Key facts
| Title | Urgent field safety notice for instruments and containers: Java pedicle screw system / Fidji cervical / lumbar cage / Wallis posterior dynamic stabilization system, Zimmer Biomet |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | instruments and containers: Java pedicle screw system / Fidji cervical / lumbar cage / Wallis posterior dynamic stabilization system, Zimmer Biomet |
| Manufacturer | Urgent field safety notice for instruments and containers: Java pedicle screw system / Fidji cervical / lumbar cage / Wallis posterior dynamic stabilization system, Zimmer Biomet |
| Models | 10-4°, SN23-100410, 2016-133, SN23-100516, SN23-105300, SN3001-1-00611, 002WNAN0000T, SN3005-2-00001, SN3005-1-00540, SN3001-1-81104, SN2036-1-00401, SN3001-1-00500 and 244 more |
| Date | Dec 16, 2016 |
| 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