International safety notice
Urgent Field Safety Notice for CardioMems Hospital and Patient Electronic System by S.. Jude Medical, Inc. - CardioMEMS
Germany / BfArM · DEU · Feb 16, 2023
Key facts
| Title | Urgent Field Safety Notice for CardioMems Hospital and Patient Electronic System by S.. Jude Medical, Inc. - CardioMEMS |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | CardioMems Hospital and Patient Electronic System |
| Manufacturer | S.. Jude Medical, Inc. - CardioMEMS |
| Models | CM1000, CM1100 |
| Date | Feb 16, 2023 |
| 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