GE OEC MEDICAL SYSTEMS INC.

Manufacturer adverse-event records for GE OEC MEDICAL SYSTEMS INC. come from the U.S. Food & Drug Administration (FDA) MAUDE database via openFDA, refreshed March 2026 - see our methodology. Not medical advice.

FDA MAUDE device safety record · 2006–2011 · heavy-book · quiet Death-code · injury-light

Injury-mix signature

GE OEC MEDICAL SYSTEMS INC. is lighter on Injury codes

Injury-coded event_type share is 0.0% (injury-light tercile) beside 0.00% Death-coded (quiet). Volume band: heavy.

What the Injury-mix reading shows for GE OEC MEDICAL SYSTEMS INC.

The standout signal for GE OEC MEDICAL SYSTEMS INC. is Injury-mix: 0.0% Injury-coded (injury-light) beside 0.00% Death-coded, on a heavy-book footprint.

As a heavy-book manufacturer, portfolio size and reporting obligations inflate absolute counts - pair GE OEC MEDICAL SYSTEMS INC. with device-family pages before treating company totals as a safety verdict. Event_type Death and Injury are one code per report; Patient Outcomes below use a separate FDA population.

Reports span 11 device types, led in this extract by Malfunction at 24,111 (99.9% of event_type total). Peak single-year volume reaches 10,193 reports across 6 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

24,130
Total Reports
1
Event-type Death
6
Injury Reports
11
Device Types

Event Types

Malfunction 24,111 (99.9%)
6 (0.0%)
Injury 6 (0.0%)
Other 6 (0.0%)
Death 1 (0.0%)

Patient Outcomes

FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.

24,123 (100.0%)
Other 4 (0.0%)
Death 1 (0.0%)
Hospitalization 1 (0.0%)

Yearly Trend

06
2006: 142
07
2007: 6,149
08
2008: 7,108
09
2009: 10,193
10
2010: 516
11
2011: 22