International safety notice
Recall of T2 Ankle Arthrodesis Nails, Stryker
Germany / BfArM · DEU · Jan 13, 2010
Key facts
| Title | Recall of T2 Ankle Arthrodesis Nails, Stryker |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of T2 Ankle Arthrodesis Nails, Stryker |
| Manufacturer | Recall of T2 Ankle Arthrodesis Nails, Stryker |
| Models | 2009-357, 18181130S, 18181030S, 18191230S, 18181230S, 18191030S |
| Date | Jan 13, 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