International safety notice
Recall of the CORE Powered Instument Driver from Stryker
Germany / BfArM · DEU · Oct 28, 2005
Key facts
| Title | Recall of the CORE Powered Instument Driver from Stryker |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the CORE Powered Instument Driver from Stryker |
| Manufacturer | Recall of the CORE Powered Instument Driver from Stryker |
| Models | 49001, 5400-050-OOOA, A-AJE-2005, 5400-050-000 |
| Date | Oct 28, 2005 |
| 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