International safety notice
Recall of the 200ml ELS Syringe for contrast media injector, Medtron AG
Germany / BfArM · DEU · Feb 14, 2014
Key facts
| Title | Recall of the 200ml ELS Syringe for contrast media injector, Medtron AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | contrast media injector, Medtron AG |
| Manufacturer | Recall of the 200ml ELS Syringe for contrast media injector, Medtron AG |
| Models | 13041617, 13091531, 13081356, 97017-20, 13071387, 13041185, 13031077, 13101521, 13061119, 13091113, 316025, 13081231 and 76 more |
| Date | Feb 14, 2014 |
| 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