International safety notice
Corrective action of the Sesamoid Plasty Workstation, Zimmer
Germany / BfArM · DEU · Dec 10, 2009
Key facts
| Title | Corrective action of the Sesamoid Plasty Workstation, Zimmer |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Corrective action of the Sesamoid Plasty Workstation, Zimmer |
| Manufacturer | Corrective action of the Sesamoid Plasty Workstation, Zimmer |
| Models | SP217, SP210, SP179, SP173, 514-395-8883, SP023, SP156, SP164, SP181, SP059, 866-978-3801, SP180 and 11 more |
| Date | Dec 10, 2009 |
| 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