International safety notice
Second Recall for Fem-Flex II Femoral Access Cannulae, Edwards Lifesciences
Germany / BfArM · DEU · Jul 8, 2009
Key facts
| Title | Second Recall for Fem-Flex II Femoral Access Cannulae, Edwards Lifesciences |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | Fem-Flex II Femoral Access Cannulae, Edwards Lifesciences |
| Manufacturer | Second Recall for Fem-Flex II Femoral Access Cannulae, Edwards Lifesciences |
| Models | 58580030, FEMII014A, 58601935, FEMII012A, 58660196, FEMII008AT, FEMII012V, 58660077, 58598254, 2009-05-04, FEMII010A, FEMII008V and 63 more |
| Date | Jul 8, 2009 |
| 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