International safety notice
Corrective action for the NAV3i Platforms and Power Box, Stryker
Germany / BfArM · DEU · Jun 18, 2014
Key facts
| Title | Corrective action for the NAV3i Platforms and Power Box, Stryker |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the NAV3i Platforms and Power Box, Stryker |
| Manufacturer | Corrective action for the NAV3i Platforms and Power Box, Stryker |
| Models | 15109, FDA-1088, FDA-0178, 15104, 15105, 15113, 15107, 269-323-7700, NAV3I, 15097, 15112, 7700-853-000 and 20 more |
| Date | Jun 18, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1,000+ Matching device models in FDA data
- 1,000+ Matching catalog numbers 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