International safety notice
Recall for the Midface Distractor, Synthes GmbH
Germany / BfArM · DEU · Feb 24, 2014
Key facts
| Title | Recall for the Midface Distractor, Synthes GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Midface Distractor, Synthes GmbH |
| Manufacturer | Recall for the Midface Distractor, Synthes GmbH |
| Models | 5359785, 1184725, 5837111, 4987627, 5206665, 4987629, 5810034, 6818437, 4987631, 6646338, 5298124, 5206675 and 31 more |
| Date | Feb 24, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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