International safety notice
Recall for the Solus Anterior Lumbar Interbody Fusion Spinal Spacer System, ALPHATEC SPINE
Germany / BfArM · DEU · Jul 14, 2011
Key facts
| Title | Recall for the Solus Anterior Lumbar Interbody Fusion Spinal Spacer System, ALPHATEC SPINE |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Solus Anterior Lumbar Interbody Fusion Spinal Spacer System, ALPHATEC SPINE |
| Manufacturer | Recall for the Solus Anterior Lumbar Interbody Fusion Spinal Spacer System, ALPHATEC SPINE |
| Models | 25500-314, 632590, 1-760-431-0289, 1.7.2011, 92008 |
| Date | Jul 14, 2011 |
| 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