International safety notice
Recall for Synex II Modular Vertebral Body Replacement System, Synthes
Germany / BfArM · DEU · Oct 27, 2009
Key facts
| Title | Recall for Synex II Modular Vertebral Body Replacement System, Synthes |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Synex II Modular Vertebral Body Replacement System, Synthes |
| Manufacturer | Recall for Synex II Modular Vertebral Body Replacement System, Synthes |
| Models | 04.808.009, L17-25, L25-33, L14-19, 04808.001, 04.808.003, L37-52, L21-29, 04.808.007, L71-97, 04.808.002, 04.808.006S and 18 more |
| Date | Oct 27, 2009 |
| 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