MEDLINE TCB228N21SRecalls & reported problems
Medline Industries, Inc. · TRANS CHAIR, 22", RDLA,SA, NYLON, 450 LB · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 6
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00193489036810), received between Sep 23, 2026 and Sep 30, 2026 — classified as 6 malfunctions.
The most frequently reported specific device problem is “Material Twisted/Bent” (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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Material Twisted/Bent3
- Fracture2
- Activation Problem1
Patient problems
- No Clinical Signs, Symptoms or Conditions6
Recent adverse event reports
The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Material Twisted/Bent
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50948808 ↗MalfunctionSep 28, 2026Material Twisted/Bent
It was reported that "while attempting to put their foot on the footrest the noticed they were bent."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50912883 ↗MalfunctionSep 24, 2026Fracture
It was reported that "The right front wheel spokes fractured right where the bearings go."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50885509 ↗MalfunctionSep 23, 2026Fracture
It was reported that "left hand side handle that holds the left arm rest on metal part has broken off the seat are and doesn not stay down. Second issue is right hand brake is slipping".
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50871208 ↗MalfunctionSep 23, 2026Material Twisted/Bent
It was reported that "The chair is bent in the back."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50870221 ↗MalfunctionSep 23, 2026Activation Problem
It was reported that "The right side legrest is no locking staying in the elevated position and will just fall."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50868046 ↗
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 MDS808200ABEMedline Industries, Inc. · CHAIR, WITH CASTERS8 reports
- GUARDIAN G1-503WCPX1Medline Industries, Inc. · CHAIR, WITH CASTERS5 reports
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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