STRYKER GMBH

Manufacturer adverse-event records for STRYKER GMBH 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 · 2013–2026 · mid-book · typical Death-code · injury-heavy

Injury-mix signature

STRYKER GMBH leans injury-heavy in event_type mix

Injury-coded event_type share is 73.1% (injury-heavy tercile) beside 0.21% Death-coded (typical). Volume band: mid.

What the Injury-mix reading shows for STRYKER GMBH

The standout signal for STRYKER GMBH is Injury-mix: 73.1% Injury-coded (injury-heavy) beside 0.21% Death-coded, on a mid-book footprint.

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

Reports span 20 device types, led in this extract by Injury at 10,624 (73.1% of event_type total). Peak single-year volume reaches 2,615 reports across 14 years. These are raw FDA submissions, not adjudicated findings. Snapshot . Verify current communications on the FDA MDR page.

14,526
Total Reports
31
Event-type Death
10,624
Injury Reports
20
Device Types

Event Types

Injury 10,624 (73.1%)
Malfunction 3,871 (26.6%)
Death 31 (0.2%)

Patient Outcomes

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

Required Intervention 7,052 (48.0%)
Other 4,896 (33.3%)
2,391 (16.3%)
R 112 (0.8%)
Hospitalization 67 (0.5%)
O 41 (0.3%)
Death 40 (0.3%)
S 35 (0.2%)
Disability 31 (0.2%)
H 30 (0.2%)
Congenital Anomaly 3 (0.0%)
D 1 (0.0%)
L 1 (0.0%)
Life Threatening 1 (0.0%)

Yearly Trend

13
2013: 23
14
2014: 60
15
2015: 609
16
2016: 620
17
2017: 724
18
2018: 1,072
19
2019: 2,509
20
2020: 2,615
21
2021: 505
22
2022: 738
23
2023: 801
24
2024: 1,652
25
2025: 2,339
26
2026: 259