International safety notice
Recall for Scorpio Fixed Femoral A/P-Sizing Guide and Scorpio Adjustable Sizing Guide, Stryker Orthopaedics
Germany / BfArM · DEU · Nov 18, 2010
Key facts
| Title | Recall for Scorpio Fixed Femoral A/P-Sizing Guide and Scorpio Adjustable Sizing Guide, Stryker Orthopaedics |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Scorpio Fixed Femoral A/P-Sizing Guide and Scorpio Adjustable Sizing Guide, Stryker Orthopaedics |
| Manufacturer | Recall for Scorpio Fixed Femoral A/P-Sizing Guide and Scorpio Adjustable Sizing Guide, Stryker Orthopaedics |
| Models | RD3S020, RD3A010A, 2010-11-26, RD2V067, GP0FÄTES, RD3AOL, RD2M080, RD2N006E, RD3A069, RD2V068, RD3N198, RD2V063 and 35 more |
| Date | Nov 18, 2010 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
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