International safety notice
Urgent Safety Notice / Recall for the Fem-Flex II™ arterial cannula sizes 16, 18 and 20 French, Edwards Lifesciences
Germany / BfArM · DEU · May 2, 2014
Key facts
| Title | Urgent Safety Notice / Recall for the Fem-Flex II™ arterial cannula sizes 16, 18 and 20 French, Edwards Lifesciences |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | the Fem-Flex II™ arterial cannula sizes 16, 18 and 20 French, Edwards Lifesciences |
| Manufacturer | Urgent Safety Notice / Recall for the Fem-Flex II™ arterial cannula sizes 16, 18 and 20 French, Edwards Lifesciences |
| Models | DFEMII018AS, DIIFEMII016A, FEMII016A, «ADD_1», FEMII020A, FEMII016AS, FEMII020AS, «ADD_2», 949.250.2525, DFEMII020AS, DIIFEMII018A, FCA-44 and 6 more |
| Date | May 2, 2014 |
| Regulator page | bfarm.de |
At a glance
- No Recall
- No Field safety notice
- 10–99 Matching device models in FDA data
- 10–99 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