International safety notice
Urgent Safety Notice for the Stryker Dekompressor® Percutaneous Discectomy Probes, Stryker
Germany / BfArM · DEU · Nov 28, 2013
Key facts
| Title | Urgent Safety Notice for the Stryker Dekompressor® Percutaneous Discectomy Probes, Stryker |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Stryker Dekompressor® Percutaneous Discectomy Probes, Stryker |
| Manufacturer | Urgent Safety Notice for the Stryker Dekompressor® Percutaneous Discectomy Probes, Stryker |
| Models | 0407-265-000, 0407-280-000, 0.103, 0407-260-000, 2.12-1, 177-179, 0.0736, 0407-251-000, 0407-266-000, 0407-281-000, RA2013-128 |
| Date | Nov 28, 2013 |
| 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