International safety notice
Recall for Trabecular Metal Acetabular Revision System Buttress Augments and Trabecular Metal Acetabular Revision System Column Buttress Augments, Zimmer Inc.
Germany / BfArM · DEU · Apr 27, 2010
Key facts
| Title | Recall for Trabecular Metal Acetabular Revision System Buttress Augments and Trabecular Metal Acetabular Revision System Column Buttress Augments, Zimmer Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Trabecular Metal Acetabular Revision System Buttress Augments and Trabecular Metal Acetabular Revision System Column Buttress Augments, Zimmer Inc. |
| Manufacturer | Recall for Trabecular Metal Acetabular Revision System Buttress Augments and Trabecular Metal Acetabular Revision System Column Buttress Augments, Zimmer Inc. |
| Models | 61143012, 00-4894-001-58, 60796674, 60530835, 60862513, 60808260, 60796679, 61081548, 004894-001-58, 60787931, 1-800-FDA-1088, 00-4894-300-00 and 44 more |
| Date | Apr 27, 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