International safety notice
Corrective action for DGDE DirectGuide Drill Extender, Implant Direct Sybron Manufacturing LLC
Germany / BfArM · DEU · Jan 28, 2016
Key facts
| Title | Corrective action for DGDE DirectGuide Drill Extender, Implant Direct Sybron Manufacturing LLC |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | DGDE DirectGuide Drill Extender, Implant Direct Sybron Manufacturing LLC |
| Manufacturer | Corrective action for DGDE DirectGuide Drill Extender, Implant Direct Sybron Manufacturing LLC |
| Models | 67475, FSCA-ID2015-11-03, 68265, 64896, 65405, 818-444-3393, 65409, 64895, 67527, 68253, 67055, 888-649-6425 and 17 more |
| Date | Jan 28, 2016 |
| 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