International safety notice
Recall of DYONICS 25 Tube Sets, Smith & Nephew
Germany / BfArM · DEU · Jun 29, 2009
Key facts
| Title | Recall of DYONICS 25 Tube Sets, Smith & Nephew |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall of DYONICS 25 Tube Sets, Smith & Nephew |
| Manufacturer | Recall of DYONICS 25 Tube Sets, Smith & Nephew |
| Models | 208-135, 0299J, 04091, 12709T, 0262254, 2778FR, 7211005, 0919K, 3048M, 78501, 3048N, 3258P and 81 more |
| Date | Jun 29, 2009 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models in FDA data
- 1–9 Matching catalog numbers 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