INVACARE SUZHOU

Manufacturer adverse-event records for INVACARE SUZHOU 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 · 2011–2025 · thin-book · typical Death-code · injury-light

Injury-mix signature

INVACARE SUZHOU is lighter on Injury codes

Injury-coded event_type share is 0.8% (injury-light tercile) beside 0.23% Death-coded (typical). Volume band: thin.

What the Injury-mix reading shows for INVACARE SUZHOU

The standout signal for INVACARE SUZHOU is Injury-mix: 0.8% Injury-coded (injury-light) beside 0.23% Death-coded, on a thin-book footprint.

As a thinner-book manufacturer, a handful of device families can swing the totals; open the device table rather than reading the company headline alone. Event_type counts are not the same population as Patient Outcomes.

Reports span 12 device types, led in this extract by Malfunction at 4,269 (98.6% of event_type total). Peak single-year volume reaches 2,662 reports across 6 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

4,329
Total Reports
10
Event-type Death
34
Injury Reports
12
Device Types

Event Types

Malfunction 4,269 (98.6%)
Injury 34 (0.8%)
16 (0.4%)
Death 10 (0.2%)

Patient Outcomes

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

Other 4,282 (98.6%)
Required Intervention 16 (0.4%)
Death 11 (0.3%)
Hospitalization 10 (0.2%)
R 8 (0.2%)
O 4 (0.1%)
Congenital Anomaly 4 (0.1%)
2 (0.0%)
Disability 2 (0.0%)
Life Threatening 2 (0.0%)
H 1 (0.0%)
L 1 (0.0%)

Yearly Trend

11
2011: 69
12
2012: 789
13
2013: 2,662
14
2014: 805
24
2024: 3
25
2025: 1