International safety notice
Recall Fogarty occlusion catheters, Edwards Lifesciences
Germany / BfArM · DEU · Jun 30, 2009
Key facts
| Title | Recall Fogarty occlusion catheters, Edwards Lifesciences |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Recall Fogarty occlusion catheters, Edwards Lifesciences |
| Manufacturer | Recall Fogarty occlusion catheters, Edwards Lifesciences |
| Models | 58597273, 58632507, 95475-512, 03.02.09, 58329183, 27.01.09, 62080822, 58457786, 15.06.07, 30.08.07, 02.09.09, 58439309 and 79 more |
| Date | Jun 30, 2009 |
| 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