MEDLINE MDS808200ABERecalls & reported problems
Medline Industries, Inc. · TRANS CHAIR,ALUM,8" WHL,19" 300 LB, BLUE · Class 1
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 00884389150835), received between Jun 24, 2026 and Sep 30, 2026 — classified as 8 malfunctions.
The most frequently reported specific device problem is “Loose or Intermittent Connection” (3 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
- Loose or Intermittent Connection3
- Material Twisted/Bent2
- Mechanical Jam2
- Fracture1
Patient problems
- No Clinical Signs, Symptoms or Conditions8
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Loose or Intermittent Connection
It was reported that "the left armrest is loose" and "one is sticking out".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50946899 ↗MalfunctionSep 30, 2026Mechanical Jam
It was reported that "the left rear wheel break of the transport chair is stuck".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50946507 ↗MalfunctionSep 30, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50945638 ↗MalfunctionSep 28, 2026Loose or Intermittent Connection
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50921417 ↗MalfunctionSep 28, 2026Mechanical Jam
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50918333 ↗MalfunctionSep 24, 2026Loose or Intermittent Connection
It was reported that "the black plastic \"u-shaped\" part that holds the seat to the frame came off and they lost it."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50882982 ↗MalfunctionAug 10, 2026Material Twisted/Bent
It was reported that FOOTREST IS BENT AND IT DOES NOT LATCH/FIT ON
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50198056 ↗MalfunctionJun 24, 2026Material Twisted/Bent
IT WAS REPORTED THAT UPON DELIVERY, THE BRAKE WAS BENT AND WILL NOT RELEASE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25611119 ↗
Other CHAIR, WITH CASTERS devices
- MEDLINE MDS808210AREMedline Industries, Inc. · CHAIR, WITH CASTERS115 reports
- MEDLINE MDS808210ABEMedline Industries, Inc. · CHAIR, WITH CASTERS75 reports
- Zippie Voyage Voyage; Voyage VIPSunrise Medical (US) LLC · Chair, With Casters1 recall9 reports
- Ki TykeKi Mobility, LLC · Chair, With Casters1 recall0 reports
- MEDLINE MDS808200KDMedline Industries, Inc. · CHAIR, WITH CASTERS22 reports
- Guardian MDS868BTRBMedline Industries, Inc. · CHAIR, WITH CASTERS8 reports
- MEDLINE TCB228N21SMedline Industries, Inc. · CHAIR, WITH CASTERS6 reports
- SARA STEDY NTB2000Arjohuntleigh AB · Chair, With Casters5 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.