MEDLINE MSCPRC31816CSRecalls & reported problems
Medline Industries, Inc. · CUSHION,W/C, GEL FOAM CUSHION,18X16X3,CS · Class 1
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00884389961868), received between Sep 24, 2026 and Sep 24, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Split, Cut or Torn” (1 report).
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 Split, Cut or Torn1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 24, 2026Material Split, Cut or Torn
It was reported that THE CUSHION COLLASSED IN THE CENTER.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50886389 ↗
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- MEDLINE MSCPRC21816CSMedline Industries, Inc. · CUSHION, WHEELCHAIR1 report
- Invacare® ContourU® Naked Back CM02BInvacare Corporation · CUSHION, WHEELCHAIR1 report
- Jay Fusion Jay Flow Fluid/Jay Air/ Jay Fluid w/CryoSunrise Medical (US) LLC · Cushion, Wheelchair1 report
- Jay Easy CushionSunrise Medical (US) LLC · Cushion, Wheelchair1 report
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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