International safety notice
Recall for the GENESIS II non-porous Tibial Baseplate, Smith & Nephew
Germany / BfArM · DEU · Feb 26, 2015
Key facts
| Title | Recall for the GENESIS II non-porous Tibial Baseplate, Smith & Nephew |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the GENESIS II non-porous Tibial Baseplate, Smith & Nephew |
| Manufacturer | Recall for the GENESIS II non-porous Tibial Baseplate, Smith & Nephew |
| Models | 14CM05996, 71420182, R-2014-20, 14CM05995, 14CT40269, 14CT39993, 14CT39992 |
| Date | Feb 26, 2015 |
| 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