MEDLINE MDS80822BRecalls & reported problems
Medline Industries, Inc. · TRANS CHAIR, DLA, SA, 22", 500 LB · Class 1
- Adverse event reports
- 4
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 00884389939348), received between Aug 11, 2026 and Sep 30, 2026 — classified as 4 malfunctions.
The most frequently reported specific device problem is “Fracture” (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
- Fracture3
- Break1
Patient problems
- No Clinical Signs, Symptoms or Conditions4
Recent adverse event reports
The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 30, 2026Fracture
It was reported that the Transport Chair fell over in the trunk while he was in a van and he noticed the hand brake had broke off.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50946023 ↗MalfunctionSep 30, 2026Fracture
It was reported that the transport chair hand brake in back has broken.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50943820 ↗MalfunctionAug 12, 2026Fracture
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50225995 ↗MalfunctionAug 11, 2026Break
It was reported that the wheelchair locking brake handle broke off and the wire came loose.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50209124 ↗
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- MEDLINE MDS808200KDMedline Industries, Inc. · CHAIR, WITH CASTERS22 reports
- Guardian MDS868BTRBMedline Industries, Inc. · CHAIR, WITH CASTERS8 reports
- MEDLINE MDS808200ABEMedline Industries, Inc. · CHAIR, WITH CASTERS8 reports
- MEDLINE TCB228N21SMedline Industries, Inc. · CHAIR, WITH CASTERS6 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.