International safety notice
Stryker Trauma AG, Division Trauma and Extremities: Corrective action for the products rHead, uHead, Sigmoid Notch, ReMotion, Radio Capitellum
Germany / BfArM · DEU · Jul 8, 2015
Key facts
| Title | Stryker Trauma AG, Division Trauma and Extremities: Corrective action for the products rHead, uHead, Sigmoid Notch, ReMotion, Radio Capitellum |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the products rHead, uHead, Sigmoid Notch, ReMotion, Radio Capitellum |
| Manufacturer | Stryker Trauma AG, Division Trauma and Extremities: Corrective action for the products rHead, uHead, Sigmoid Notch, ReMotion, Radio Capitellum |
| Models | 23946603, 19125-S2, 18834, 23917101, 19720-S2, 19802-S2, 310-0013, 19917-S2, R23493402, 310-0003, 19865-S2, 22217301 and 797 more |
| Date | Jul 8, 2015 |
| 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