MEDLINE MSCPRC21816CSRecalls & reported problems
Medline Industries, Inc. · CUSHION,W/C, GEL FOAM CUSHION,18X16X2,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 00888277715854), received between Sep 29, 2026 and Sep 29, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Lack of Effect” (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
- Lack of Effect1
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 29, 2026Lack of Effect
It was reported that the material on the inside is causing the cushion to be bumpy.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50937037 ↗
Other CUSHION, WHEELCHAIR devices
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- Drive RTL1493COMDrive Devilbiss Healthcare · CUSHION, WHEELCHAIR3 deaths3 reports
- Matrx-Vi Cushion MA-ViMotion Concepts Inc · Cushion, Wheelchair2 reports
- Matrx E2 Standard Back E2SMotion Concepts 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
- MEDLINE MSCPRC31816CSMedline Industries, Inc. · 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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