International safety notice
Recall for the LEXA® femoral components, C2F IMPLANTS
Germany / BfArM · DEU · Jul 14, 2015
Key facts
| Title | Recall for the LEXA® femoral components, C2F IMPLANTS |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the LEXA® femoral components, C2F IMPLANTS |
| Manufacturer | Recall for the LEXA® femoral components, C2F IMPLANTS |
| Models | IMP13011, 011281002000, 011281010000, 20140923, 03-25-02-72-89, IMP03012, 011406012000, 011281012000, «RUE2», 3250A, 52800, 011281014000 and 24 more |
| Date | Jul 14, 2015 |
| 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