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Vital Signs
Carefusion Finland 320 Oy · Model 545344 · UDI-DI 10885403268656
MLD
Prescription
10
510(k) clearances
33
Adverse events (4 deaths)
2
Recalls
48
Facilities
Description
300-Series ECG Leadwire, Individual Replacement, Black LA, Grabber, AHA, 75cm/30in
Recalls
| Date | Firm | Reason |
|---|---|---|
| 2006-02-06 | GE Medical Systems Information Tecnology | GE Healthcare (Datex-Ohmeda) S/5 Critical Care Monitor and S/5 Compact Critical Care Monitor with L-CICU01, L-CICU02A, L-ICU05 & L-ICUO5A software had an issue where the Heart Rate |
| 2006-02-06 | GE Medical Systems Information Tecnology | GE Healthcare (Datex-Ohmeda) S/5 Critical Care Monitor and S/5 Compact Critical Care Monitor with L-CICU01, L-CICU02A, L-ICU05 & L-ICUO5A software had an issue where the Heart Rate |
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Get your free API keyRead the docsData compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.
