International safety notice
Recall for Craniomaxillofacial (CMF) Distraction System, DePuy Synthes GmbH
Germany / BfArM · DEU · May 15, 2014
Key facts
| Title | Recall for Craniomaxillofacial (CMF) Distraction System, DePuy Synthes GmbH |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Craniomaxillofacial (CMF) Distraction System, DePuy Synthes GmbH |
| Manufacturer | Recall for Craniomaxillofacial (CMF) Distraction System, DePuy Synthes GmbH |
| Models | 7306561, 04.315.023, 7476791, 7266967, IS10385, 64541, 7418848, 6651388, 7422705, IS10400, 6410544, 7556150 and 135 more |
| Date | May 15, 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