PlainHospital

AGFA HEALTHCARE CORP

Manufacturer adverse-event records for AGFA HEALTHCARE CORP 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 · 2010–2015 · mid-book · quiet Death-code · injury-light

Injury-mix signature

AGFA HEALTHCARE CORP is lighter on Injury codes

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

What the Injury-mix reading shows for AGFA HEALTHCARE CORP

The standout signal for AGFA HEALTHCARE CORP is Injury-mix: 0.0% Injury-coded (injury-light) beside 0.00% Death-coded, on a mid-book footprint.

Mid-pack volume still shows a clear device fingerprint; the table below is the actionable layer for AGFA HEALTHCARE CORP. Event_type Death/Injury codes differ from patient-outcome rows - see methodology.

Reports span 4 device types, led in this extract by Malfunction at 8,980 (100.0% of event_type total). Peak single-year volume reaches 8,831 reports across 6 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

8,981
Total Reports
0
Event-type Death
0
Injury Reports
4
Device Types

Event Types

Malfunction 8,980 (100.0%)
Other 1 (0.0%)

Patient Outcomes

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

8,981 (100.0%)

Devices (4)

Device Reports
System, Image Processing, Radiological 8,972
Catheter, Sampling, Chorionic Villus 4
Device, Digital Image Storage, Radiological 4
Electrocardiograph 1

Yearly Trend

10
2010: 1
11
2011: 1
12
2012: 3
13
2013: 127
14
2014: 8,831
15
2015: 18

Read our methodology - how this data is sourced, computed, and verified.