International safety notice
Recall for the MGuard Prime Coronary Stent System Embolic Protective Stent (EPS), InspireMD Ltd.
Germany / BfArM · DEU · May 28, 2014
Key facts
| Title | Recall for the MGuard Prime Coronary Stent System Embolic Protective Stent (EPS), InspireMD Ltd. |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the MGuard Prime Coronary Stent System Embolic Protective Stent (EPS), InspireMD Ltd. |
| Manufacturer | Recall for the MGuard Prime Coronary Stent System Embolic Protective Stent (EPS), InspireMD Ltd. |
| Models | MGP4038, 0800-3305098, MGP2523, MGP3208, MGP4018, MGP2728, MGP2713, MGP3513, MGP3033, 0800-940133, MGP3223, MGP3228 and 36 more |
| Date | May 28, 2014 |
| 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