Medline MDT216904Recalls & reported problems
Medline Industries, Inc. · TOWEL,OR,DSP,NS,BLUE,LOW-LINT,400/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 40888277323637), received between May 7, 2026 and May 7, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Material Erosion” (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 Erosion1
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.
MalfunctionMay 7, 2026Material Erosion
CUSTOMER STATES WE HAVE AND OR TOWEL THAT WE USE IN SPD BUT IT IS MADE OF COTTON AND IS LEAVING PIECES OF THE COTTON ON STERILE TRAY AND INSTRUMENTS.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25116871 ↗
Other FIBER, MEDICAL, ABSORBENT devices
- MEDLINE MDT2168204Medline Industries, Inc. · FIBER, MEDICAL, ABSORBENT18 reports
- MEDLINE MDT2168284Medline Industries, Inc. · FIBER, MEDICAL, ABSORBENT14 reports
- MEDLINE MDT2168286Medline Industries, Inc. · FIBER, MEDICAL, ABSORBENT11 reports
- MEDLINE MDT2168304Medline Industries, Inc. · FIBER, MEDICAL, ABSORBENT6 reports
- MEDLINE MDT2168210Medline Industries, Inc. · FIBER, MEDICAL, ABSORBENT5 reports
- Curity 6939Cardinal Health, Inc. · FIBER, MEDICAL, ABSORBENT4 reports
- CARDINAL HEALTH 28700-006Cardinal Health 200, LLC · FIBER, MEDICAL, ABSORBENT4 reports
- MEDLINE MDT2168202Medline Industries, Inc. · FIBER, MEDICAL, ABSORBENT4 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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