International safety notice
Recall for the PathFinder NXT Pivoting Percutaneous Rod Holder Instrument, Zimmer Inc.
Germany / BfArM · DEU · Jul 2, 2012
Key facts
| Title | Recall for the PathFinder NXT Pivoting Percutaneous Rod Holder Instrument, Zimmer Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the PathFinder NXT Pivoting Percutaneous Rod Holder Instrument, Zimmer Inc. |
| Manufacturer | Recall for the PathFinder NXT Pivoting Percutaneous Rod Holder Instrument, Zimmer Inc. |
| Models | 866-7746368, 3564-100, 1-800-FDA-1088, 208529787, 952-832-5600, 866-774-6368, 20852-9787, L1554, 55439, 1-800-FDA-0178, 3564-1, 258-0995 and 4 more |
| Date | Jul 2, 2012 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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