MEDLINE INDUSTRIES, INC. DYNJT3687Recalls & reported problems
Medline Industries, Inc. · C SECTION PACK · Class 2
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10198459345913), received between May 13, 2026 and May 27, 2026 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Device Dislodged or Dislocated” (2 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Device Dislodged or Dislocated2
- Loss of or Failure to Bond1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 27, 2026Device Dislodged or Dislocated
THE DRAPE HAS NOT STUCK TO THE PATIENT AND HAS MADE A MESS ALL OVER THE DOCTORS AND FLOOR. THE DRAPE DOES NOT STICK TO THE PATIENT AND WE WOULD LIKE A DIFFERENT PACK THAT WORKS THE WAY IT IS SUPPOSED TO WORK. THE DRAPES ARE SUPPOSED TO STICK TO THE PATIENT AND IT IS NOT STICKING TO THE PATIENT. THE DRAPE DOES NOT STICK ON THE PATIENT AND DOESN'T SERVE ITS PURPOSE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25307168 ↗MalfunctionMay 27, 2026Device Dislodged or Dislocated
THE DRAPE HAS NOT STUCK TO THE PATIENT AND HAS MADE A MESS ALL OVER THE DOCTORS AND FLOOR. THE DRAPE DOES NOT STICK TO THE PATIENT AND WE WOULD LIKE A DIFFERENT PACK THAT WORKS THE WAY IT IS SUPPOSED TO WORK. THE DRAPES ARE SUPPOSED TO STICK TO THE PATIENT AND IT IS NOT STICKING TO THE PATIENT. THE DRAPE DOES NOT STICK ON THE PATIENT AND DOESN'T SERVE ITS PURPOSE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25307144 ↗MalfunctionMay 13, 2026Loss of or Failure to Bond
IT WAS REPORTED ON (B)(6) THAT DURING USE OF A DRAPE IN THE C-SECTION PACK, THE ADHESIVE DID NOT ADEQUATELY ADHERE TO THE PATIENT'S SKIN. AS A RESULT, BLOOD AND OTHER BODILY FLUIDS WERE OBSERVED LEAKING BENEATH THE DRAPE AND ONTO THE FLOOR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 25164187 ↗
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- Medline Industries, Inc. DYNJ904653GMedline Industries, Inc. · Cesarean section tray3 recalls0 reports
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- Medline Industries, Inc. DYNJ33059BMedline Industries, Inc. · Cesarean section tray3 recalls0 reports
- Medline Industries, Inc. DYNJ47808FMedline Industries, Inc. · Cesarean section tray3 recalls0 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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