Wings P3036CRecalls & reported problems
Cardinal Health, Inc. · Quilted Premium Comfort Underpad,Extra Heavy · Class 1
Data updated Oct 13, 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 10884521141803), received between Feb 7, 2020 and Feb 7, 2020 — 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. How this data works · Data updated Oct 13, 2026.
Most reported problems
Device problems
- Material Split, Cut or Torn1
Patient problems
- No Consequences Or Impact To Patient1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionFeb 7, 2020Material Split, Cut or Torn; Material Split, Cut or Torn
THE CUSTOMER REPORTED THAT THE UNDERPAD RIPPED WHEN TURNING A (B)(6) POUND MALE PATIENT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9682157 ↗
Other BEDDING, DISPOSABLE, MEDICAL devices
- Wings P3036PSCardinal Health, Inc. · BEDDING, DISPOSABLE, MEDICAL1 report
- Sage AirTAP LC 7289Sage Products, LLC · BEDDING, DISPOSABLE, MEDICAL1 report
- Curaplex MS-42210Bound Tree Medical, LLC · BEDDING, DISPOSABLE, MEDICAL1 report
- Wings 959Cardinal Health, Inc. · BEDDING, DISPOSABLE, MEDICAL1 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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