International safety notice
Lot Recall for Genesis II Tibial Drill Guide, Smith & Nephew
Germany / BfArM · DEU · Apr 30, 2010
Key facts
| Title | Lot Recall for Genesis II Tibial Drill Guide, Smith & Nephew |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Genesis II Tibial Drill Guide, Smith & Nephew |
| Manufacturer | Lot Recall for Genesis II Tibial Drill Guide, Smith & Nephew |
| Models | 二気鸞こ」を3・第第第い、をに, をこを3こにを, 901-566-7975, 08JM07761A, R1006, みイい0ト, 38118, 71440238, 08JM07761, 峯攣し。ド第=しこ二に、毳鵞朝の、こ・~当三膨第1第、, を3をいをを |
| Date | Apr 30, 2010 |
| 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