International safety notice
Corrective action of several batches of LEGION COCR Constrained Femoral device, Smith & Nephew
Germany / BfArM · DEU · Nov 7, 2014
Key facts
| Title | Corrective action of several batches of LEGION COCR Constrained Femoral device, Smith & Nephew |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Corrective action of several batches of LEGION COCR Constrained Femoral device, Smith & Nephew |
| Manufacturer | Corrective action of several batches of LEGION COCR Constrained Femoral device, Smith & Nephew |
| Models | 14FM07393, 71426003, 14EM23395, 71425005, 71426007, 71426005, 71426006, 14EM23390, 14FM20203, 14DM22269, 14FM05730, 14FM17740 and 11 more |
| Date | Nov 7, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 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