International safety notice
Urgent Field Safety Notice for GENESIS II NON-POROUS TIBIAL BASEPLATE by Smith & Nephew, Inc., Orthopaedics
Germany / BfArM · DEU · Aug 12, 2020
Key facts
| Title | Urgent Field Safety Notice for GENESIS II NON-POROUS TIBIAL BASEPLATE by Smith & Nephew, Inc., Orthopaedics |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | GENESIS II NON-POROUS TIBIAL BASEPLATE |
| Manufacturer | Smith & Nephew, Inc., Orthopaedics |
| Models | G1925654, G1925682, 20AT33571, G1925713, 20BT33886, 20BT33861, G1926271, G1923964, G1923992, G1924451, G1925194, 20BT33879 and 121 more |
| Date | Aug 12, 2020 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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