International safety notice
Recall of VarioFit Classic cementfree hip prostheses, aap Implantate AG
Germany / BfArM · DEU · Apr 4, 2017
Key facts
| Title | Recall of VarioFit Classic cementfree hip prostheses, aap Implantate AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of VarioFit Classic cementfree hip prostheses, aap Implantate AG |
| Manufacturer | Recall of VarioFit Classic cementfree hip prostheses, aap Implantate AG |
| Models | 3115-02, 49-30-75019-111, 3118-02, 3114-02, 12099, 3111-02, 3110-01, E49-30, 00534, 3116-02, 3110-02, 3118-01 and 15 more |
| Date | Apr 4, 2017 |
| 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