International safety notice
Stryker recalls the Scorpio Total Knee Replacement System
Germany / BfArM · DEU · Aug 26, 2005
Key facts
| Title | Stryker recalls the Scorpio Total Knee Replacement System |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Stryker recalls the Scorpio Total Knee Replacement System |
| Manufacturer | Stryker recalls the Scorpio Total Knee Replacement System |
| Models | DR.-HOMET•SOKER-PLAT2, 2065-837-127, K04W537, RA-2005-044, 16964, RA-200S-040, 47228, 17-ALJG-20ES, 17-AIJG-2ØØS, GCSCH4FTSIUHRCR, 837-837, 70-4107R and 11 more |
| Date | Aug 26, 2005 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 100–999 Matching device models in FDA data
- 100–999 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