International safety notice
Recall of all EIUS Tibial and Femur Implants and of all Titan EIUS Femur Implants, Stryker
Germany / BfArM · DEU · Sep 30, 2011
Key facts
| Title | Recall of all EIUS Tibial and Femur Implants and of all Titan EIUS Femur Implants, Stryker |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of all EIUS Tibial and Femur Implants and of all Titan EIUS Femur Implants, Stryker |
| Manufacturer | Recall of all EIUS Tibial and Femur Implants and of all Titan EIUS Femur Implants, Stryker |
| Models | T636-2-003, T636-2-013, T636-2-012, OMT2011-1, T636-2-014, T636-2-011, T636-2-002, T636-2-005, T636-2-015, T636-2-001, T636-2-004 |
| Date | Sep 30, 2011 |
| 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