International safety notice
Recall of the DYONICS 25 Patient Tube Set, Smith & Nephew
Germany / BfArM · DEU · Feb 11, 2014
Key facts
| Title | Recall of the DYONICS 25 Patient Tube Set, Smith & Nephew |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of the DYONICS 25 Patient Tube Set, Smith & Nephew |
| Manufacturer | Recall of the DYONICS 25 Patient Tube Set, Smith & Nephew |
| Models | 7211008, R-2014-02, 50426552 |
| Date | Feb 11, 2014 |
| 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