International safety notice
Recall for NexGen Complete Knee Solution MIS Total Knee Procedure Tibial Broach Impactor, Zimmer Inc.
Germany / BfArM · DEU · Jul 18, 2008
Key facts
| Title | Recall for NexGen Complete Knee Solution MIS Total Knee Procedure Tibial Broach Impactor, Zimmer Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | NexGen Complete Knee Solution MIS Total Knee Procedure Tibial Broach Impactor, Zimmer Inc. |
| Manufacturer | Recall for NexGen Complete Knee Solution MIS Total Knee Procedure Tibial Broach Impactor, Zimmer Inc. |
| Models | 60314122, 60679633, 60436520, 60384503, 60331361, 60859085, 60715232, 60827029, 60943652, 60783673, 60525081, 60353140 and 47 more |
| Date | Jul 18, 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