International safety notice
Recall Xvoid Kyphoplastie Systems, Sintea Biotech
Germany / BfArM · DEU · Mar 31, 2008
Key facts
| Title | Recall Xvoid Kyphoplastie Systems, Sintea Biotech |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall Xvoid Kyphoplastie Systems, Sintea Biotech |
| Manufacturer | Recall Xvoid Kyphoplastie Systems, Sintea Biotech |
| Models | 01925740183, 02499, 02488, 175.600, 02497, ON125, 02487, 39.02.38.204.222, 02474, 39.02.38.204.230, 20021, 02532 and 12 more |
| Date | Mar 31, 2008 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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