International safety notice
Recall for SafeSheath® CSG® Coronary Sinus Guide Braided Core Hemostatic Introducer, SafeSheath® Worley Telescopic Braided Series and Situs LDS 2 Lead Delivery System, GE Healthcare
Germany / BfArM · DEU · Feb 27, 2012
Key facts
| Title | Recall for SafeSheath® CSG® Coronary Sinus Guide Braided Core Hemostatic Introducer, SafeSheath® Worley Telescopic Braided Series and Situs LDS 2 Lead Delivery System, GE Healthcare |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | SafeSheath® CSG® Coronary Sinus Guide Braided Core Hemostatic Introducer, SafeSheath® Worley Telescopic Braided Series and Situs LDS 2 Lead Delivery System, GE Healthcare |
| Manufacturer | Recall for SafeSheath® CSG® Coronary Sinus Guide Braided Core Hemostatic Introducer, SafeSheath® Worley Telescopic Braided Series and Situs LDS 2 Lead Delivery System, GE Healthcare |
| Models | S31045, S31779X1, S33161X1, S25489, S26539, S33076, S31005X1, S33398, S33067, S31535X1, 1-866-446-3003, S26881 and 179 more |
| Date | Feb 27, 2012 |
| 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