International safety notice
Architect i2000 system
Swiss / SwissMedic · CHE · Dec 18, 2007
Key facts
| Title | Architect i2000 system |
|---|---|
| Regulator | Swiss / SwissMedic |
| Country | CHE |
| Brand | Architect i2000 system |
| Manufacturer | Abbott Ireland Diagnostic Division |
| Models | i2000, 768’44’52, 8C8901, 768’44, 7K6020, 3M7401, 7K6030, 768’44’22, 7K6025, i2000SR |
| Event type | Safety Notice |
| Date | Dec 18, 2007 |
| Regulator page | fsca.swissmedic.ch |
At a glance
- No Recall
- Yes 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