International safety notice
Urgent Field Safety Notice for CASE / CardioSoft Cardiac Testing System by GE Medical Systems Information Technologies
Germany / BfArM · DEU · Jun 22, 2021
Key facts
| Title | Urgent Field Safety Notice for CASE / CardioSoft Cardiac Testing System by GE Medical Systems Information Technologies |
|---|---|
| Regulator | Germany / BfArM |
| Country | DEU |
| Brand | CASE / CardioSoft Cardiac Testing System |
| Manufacturer | GE Medical Systems Information Technologies |
| Models | 00840682105156, 53188, 00840682144179, V6.6X, 00840682105170, 00840682123679, 00840682105088, 2008-R2, WINDOWS-7-SUPPORT-ENDED-ONJANUARY-14-2020-B75D4580-2CC7-895A-2C9C-1466D9A53962, V6.7X, 30098-2, END-OF-SUPPORT-WINDOWS-SERVER-2008-2008R2 |
| Date | Jun 22, 2021 |
| 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