International safety notice
Lot Recall of the Facet Wedge Trial Implant w/rasp small cannulated, Synthes GmbH
Germany / BfArM · DEU · Nov 12, 2012
Key facts
| Title | Lot Recall of the Facet Wedge Trial Implant w/rasp small cannulated, Synthes GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Lot Recall of the Facet Wedge Trial Implant w/rasp small cannulated, Synthes GmbH |
| Manufacturer | Lot Recall of the Facet Wedge Trial Implant w/rasp small cannulated, Synthes GmbH |
| Models | 9656601, 03.630.130, 1219945, 96561, SWN-1ESO |
| Date | Nov 12, 2012 |
| 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