International safety notice
Recall of several lots of the LifeStent Solo Vascular Stent System. The recall is only for products of the old design, Angiomed GmbH & Co. Medizintechnik KG
Germany / BfArM · DEU · Nov 19, 2013
Key facts
| Title | Recall of several lots of the LifeStent Solo Vascular Stent System. The recall is only for products of the old design, Angiomed GmbH & Co. Medizintechnik KG |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | products of the old design, Angiomed GmbH & Co. Medizintechnik KG |
| Manufacturer | Recall of several lots of the LifeStent Solo Vascular Stent System. The recall is only for products of the old design, Angiomed GmbH & Co. Medizintechnik KG |
| Models | Q2013-006, 76227 |
| Date | Nov 19, 2013 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 1–9 Matching device models 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