International safety notice
Recall for the product CERAFIT REVISION - Diaphyseal stem - Cementless, Ceraver
Germany / BfArM · DEU · Jun 12, 2014
Key facts
| Title | Recall for the product CERAFIT REVISION - Diaphyseal stem - Cementless, Ceraver |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the product CERAFIT REVISION - Diaphyseal stem - Cementless, Ceraver |
| Manufacturer | Recall for the product CERAFIT REVISION - Diaphyseal stem - Cementless, Ceraver |
| Models | 12747, FSCA_CER2014-01, 12745, 12746, 12744, 12748, 12759, 12741, 12743, 12749, 7206-4, 12742 and 1 more |
| Date | Jun 12, 2014 |
| 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