Medline MDSMELSCALERecalls & reported problems
Medline Industries, Inc. · SCALE, FOR PATIENT LIFTS, 700 LB. CAP · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10888277339439), received between Aug 31, 2026 and Aug 31, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Calibration Problem” (2 reports).
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Calibration Problem2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 31, 2026Calibration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50530713 ↗MalfunctionAug 31, 2026Calibration Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50520139 ↗
Other SCALE, PATIENT devices
- Welch Allyn, Inc. 901110Welch Allyn, Inc. · SCALE, PATIENT3 reports
- DRIVE FLSCALEDrive Devilbiss Healthcare · SCALE, PATIENT1 report
- Welch Allyn, Inc. 901110Welch Allyn, Inc. · SCALE, PATIENT1 report
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.