International safety notice
Recall for syringes intended for contrast media application, Medtron AG
Germany / BfArM · DEU · Nov 21, 2011
Key facts
| Title | Recall for syringes intended for contrast media application, Medtron AG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | contrast media application, Medtron AG |
| Manufacturer | Recall for syringes intended for contrast media application, Medtron AG |
| Models | 102079, 106991, 316025, 97017, 102095, 316026, 106009, 102022, 103027, 103991, 103045, 103064 and 16 more |
| Date | Nov 21, 2011 |
| 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