Lift, Patient, Non-Ac-Powered
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 §880.5510 (General Hospital panel).
FDA MAUDE casebook
openFDA event book Lift, Patient, Non-Ac-Powered MID-BOOK · MAUDE
#174 of 1000 · 14,697 reports · 1993–2026
- BOOK 14,697 reports
- RANK #174 of 1000
- DEATH 423 death-typed
- INJ 2,850 injury-typed
- MALF 9,819 malfunction
- SPAN 1993–2026
- PEAK 2013: 1,923
- PHOTO Appliance
Nearest event-volume peer: Appliance, Fixation, Spinal Interlaminal (130 report gap)
Lift, Patient, Non-Ac-Powered sits #174 of 1000 among tracked device types with 14,697 MAUDE reports spanning 1993–2026. 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 → · Lead manufacturer → · Similar-volume device →
Injury-coded reports sit below the device-type norm
Lift, Patient, Non-Ac-Powered carries 19.4% INJURY-coded reports, 10.9pp below the 1,000-device-type mean, the widest gap of its three event codes. Codes are report labels, not adjudicated causation.
- DEATH 2.9% corpus 1.5% · above corpus mean (+1.4 pp)
- INJ 19.4% corpus 30.3% · below corpus mean (-10.9 pp)
- MALF 66.8% corpus 64.8% · above corpus mean (+2.0 pp)
Lead product-problem code Break is 14% of coded problems · Lead manufacturer INVACARE SUZHOU accounts for 45% of manufacturer-tagged reports · Top event location is 61% of location-tagged rows .
Lift, Patient, Non-Ac-Powered in the event-volume neighbourhood
FDA MAUDE report totals among this device type and nearest nationwide peers
- Tube Tracheos…
Tube Tracheostomy And Tube Cuff
14,927 reports
- Pump
Pump, Infusion, Enteral
14,912 reports
- Lift (this)
Lift, Patient, Non-Ac-Powered
14,697 reports
- Appliance
Appliance, Fixation, Spinal Interlaminal
14,567 reports
- Pulse Generat…
Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)
14,494 reports
- Device
Device, Vascular, For Promoting Embolization
14,423 reports
What this shows Lift, Patient, Non-Ac-Powered carries 14,697 MAUDE reports, ranked #174 of 1000.
Event Types
Patient Outcomes
FDA patient-outcome codes (separate from event_type). Percentages use this chart's row total.
Top Product Problems
Yearly Trend
Reports in 2025 (438) held close to the prior two-year average of 357.
Related Entities for Lift, Patient, Non-Ac-Powered
Top Manufacturers
Event Locations
Nationwide devices with a comparable volume-and-death footprint
Two openFDA-derived peer sets for Lift, Patient, Non-Ac-Powered: 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 (14,697 here).
Similar death-typed counts
Nearest other device types by death-typed report count (423 here), distinct from the volume row.
Read our methodology - how this data is sourced, computed, and verified.
Disclaimer: MAUDE figures for Lift, Patient, Non-Ac-Powered 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 Lift, Patient, Non-Ac-Powered; 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.