International safety notice
Corrective action - Manufacturer IFU replacement for the VariLase® Endovenous Laser Fibers and Procedure Kits, Vascular Solutions Inc.
Germany / BfArM · DEU · Jun 17, 2015
Key facts
| Title | Corrective action - Manufacturer IFU replacement for the VariLase® Endovenous Laser Fibers and Procedure Kits, Vascular Solutions Inc. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the VariLase® Endovenous Laser Fibers and Procedure Kits, Vascular Solutions Inc. |
| Manufacturer | Corrective action - Manufacturer IFU replacement for the VariLase® Endovenous Laser Fibers and Procedure Kits, Vascular Solutions Inc. |
| Models | IFU’SARETOBEREPLACEDFORVARIͲLASEPROCEDUREKITSWITHLOTNUMBERSBETWEEN565760AND580413, INDICATE“0”WHEREAPPLICABLE, STEP2, STEP4, VISITTOREPLACEIFU’SFORDEVICESIDENTIFIEDINSTEP3, PLEASECOMPLETETHESESTEPSWITHIN10DAYSOFRECEIVINGTHIS, STEP1, STEP5 |
| Date | Jun 17, 2015 |
| 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