2026 data FDA MAUDE openFDA FDA Class I

Patient Bed With Canopy/Restraints

Adverse-event figures are drawn from the U.S. Food & Drug Administration (FDA) MAUDE database, refreshed March 2026, see our methodology.

OpenFDA device adverse-event casebook.

FDA Class I (lowest regulatory risk tier, general controls), regulated under 21 CFR §880.6760 (General Hospital panel).

FDA MAUDE casebook

openFDA event book Patient Bed With Canopy/Restraints LIGHT-BOOK · MAUDE

#924 of 1000 · 462 reports · 2004–2026

  • BOOK 462 reports
  • RANK #924 of 1000
  • DEATH 8 death-typed
  • INJ 17 injury-typed
  • MALF 435 malfunction
  • SPAN 2004–2026
  • PEAK 2025: 87
  • PHOTO Urinometer, Electrical

Nearest event-volume peer: Urinometer, Electrical (2 report gap)

Patient Bed With Canopy/Restraints sits #924 of 1000 among tracked device types with 462 MAUDE reports spanning 2004–2026. Rank counts report volume, not confirmed device fault. Event_type Death / Injury / Malfunction are one code per report — not the same population as patient-outcome rows ( methodology). Read with this device → · Similar-volume device →

Malfunction reports run above the device-type norm

Patient Bed With Canopy/Restraints carries 94.2% MALFUNCTION-coded reports, 29.3pp above the 1,000-device-type mean, the widest gap of its three event codes. Codes are report labels, not adjudicated causation.

  • DEATH 1.7% corpus 1.5% · near corpus mean (+0.2 pp)
  • INJ 3.7% corpus 30.3% · below corpus mean (-26.6 pp)
  • MALF 94.2% corpus 64.8% · above corpus mean (+29.3 pp)

Lead product-problem code Material Separation is 25% of coded problems · Top event location is 86% of location-tagged rows .

Patient Bed With Canopy/Restraints in the event-volume neighbourhood

FDA MAUDE report totals among this device type and nearest nationwide peers

reports

What this shows Patient Bed With Canopy/Restraints carries 462 MAUDE reports, ranked #924 of 1000.

Source FDA MAUDE via openFDA, aggregated by PlainHospital As of August 2026

Event Types

Malfunction 435 (94.2%)
Injury 17 (3.7%)
Death 8 (1.7%)
1 (0.2%)
Other 1 (0.2%)

Patient Outcomes

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

430 (90.5%)
Required Intervention 13 (2.7%)
Death 8 (1.7%)
Other 7 (1.5%)
L 3 (0.6%)
O 3 (0.6%)
R 3 (0.6%)
Hospitalization 3 (0.6%)
H 2 (0.4%)
S 2 (0.4%)
Life Threatening 1 (0.2%)

Top Product Problems

Material Separation 120
Break 89
Mechanical Problem 38
Material Split, Cut or Torn 33
Component Missing 30
Failure to Align 25
Detachment Of Device Component 21
Appropriate Device Problem Term/Code Not Available 16
Device Operates Differently Than Expected 16
Insufficient Device Problem Information 16
Material Integrity Problem 15
Fail-Safe Did Not Operate 12
Torn Material 11
Use of Device Problem 11
Improper or Incorrect Procedure or Method 7
Adverse Event Without Identified Device or Use Problem 6
Difficult to Open or Close 5
Mechanics Altered 5
Defective Component 4
Fail-Safe Problem 4

Yearly Trend

04
2004: 1
10
2010: 1
12
2012: 53
13
2013: 80
14
2014: 53
15
2015: 9
16
2016: 7
17
2017: 6
18
2018: 15
19
2019: 16
20
2020: 6
21
2021: 5
22
2022: 28
23
2023: 7
24
2024: 31
25
2025: 87
26
2026: 57

Reports rose to 87 in 2025, up from an average of 19 in the two years before - a recent-year increase, not a lifetime pattern.

Related Entities for Patient Bed With Canopy/Restraints

Event Locations

398 (86.1%)
I 57 (12.3%)
HOSPITAL 4 (0.9%)
HOME 2 (0.4%)
NO INFORMATION 1 (0.2%)

Nationwide devices with a comparable volume-and-death footprint

Two openFDA-derived peer sets for Patient Bed With Canopy/Restraints: nearest by total report volume and nearest by death-typed count, each floored at ≥100 reports so the neighborhoods stay in the advertised mass.

Similar report volume

Nearest other device types by FDA MAUDE report count (462 here).

Similar death-typed counts

Nearest other device types by death-typed report count (8 here), distinct from the volume row.

Disclaimer: MAUDE figures for Patient Bed With Canopy/Restraints are informational only and are not clinical advice. Report codes do not prove device causation. Consult a qualified clinician before acting on this data.

Every figure on PlainHospital is rendered directly from federal source data, no number is typed in by an editor. Event-type mix on this page is computed from FDA MAUDE codes for Patient Bed With Canopy/Restraints; corpus means use device types with ≥100 reports. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of August 2026.