International safety notice
Recall for RT-Plus Modular Stepped Drill and RT-Plus Modular Tibial Drill Guide, Smith & Nephew Orthopaedics
Germany / BfArM · DEU · Jun 1, 2011
Key facts
| Title | Recall for RT-Plus Modular Stepped Drill and RT-Plus Modular Tibial Drill Guide, Smith & Nephew Orthopaedics |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | RT-Plus Modular Stepped Drill and RT-Plus Modular Tibial Drill Guide, Smith & Nephew Orthopaedics |
| Manufacturer | Recall for RT-Plus Modular Stepped Drill and RT-Plus Modular Tibial Drill Guide, Smith & Nephew Orthopaedics |
| Models | 872149, 871901, 75015047, 240445, 871158, 871221, 870869, 873927, 872700, 873887, 240449, 871268 and 4 more |
| Date | Jun 1, 2011 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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