International safety notice
Recall for the NexGen® Complete Knee Solution PRI - Femoral and Provisional Impactor/Extractor, Zimmer Inc.
Germany / BfArM · DEU · Apr 27, 2011
Key facts
| Title | Recall for the NexGen® Complete Knee Solution PRI - Femoral and Provisional Impactor/Extractor, Zimmer Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the NexGen® Complete Knee Solution PRI - Femoral and Provisional Impactor/Extractor, Zimmer Inc. |
| Manufacturer | Recall for the NexGen® Complete Knee Solution PRI - Femoral and Provisional Impactor/Extractor, Zimmer Inc. |
| Models | 00-5901-026-00, 61542077, 61516146, 61610343, 61690174, 61565681, 61637191, 61584438, 61645115, 1-800-FDA1088, 1-800FDA-0178, 1-800-FDA-1088 and 15 more |
| Date | Apr 27, 2011 |
| 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