International safety notice
Recall for T2 OFx Tibia Nails, Stryker
Germany / BfArM · DEU · Mar 25, 2008
Key facts
| Title | Recall for T2 OFx Tibia Nails, Stryker |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | T2 OFx Tibia Nails, Stryker |
| Manufacturer | Recall for T2 OFx Tibia Nails, Stryker |
| Models | K7782S3, K778275, 47228, 10900, 18270839S, 41298, 16964, 18270837S, RA-2008-I4, G«CHIFT3NHRER, 47298, 18270834S and 26 more |
| Date | Mar 25, 2008 |
| 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