Medline DYNJP2499Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10080196739462), received between Dec 9, 2021 and Sep 29, 2026 — classified as 4 malfunctions.

The most frequently reported specific device problem is “Difficult to Remove” (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.

Most reported problems

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 29, 2026Material Puncture/Hole; Material Split, Cut or Torn

  It was reported that Customer receieved 1EA of DYNJP2499 opened the package damaged. The inside cover is ripped, bu the outside plastic was intact.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50934899 ↗
• MalfunctionSep 14, 2026Unsealed Device Packaging

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50756603 ↗
• MalfunctionSep 11, 2026Loss of or Failure to Bond

  It was reported that "While draping, when removing cover to show adhesive strip, the adhesive came off with cover."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50734028 ↗
• MalfunctionDec 9, 2021Difficult to Remove; Patient-Device Incompatibility

  STERILE BLUE FILM "U" DRAPE CAUSED BRUISING TO PATIENT'S UPPER ARM BELOW TOURNIQUET. THE MEDLINE DRAPE PIECE IS SO STICKY, ALMOST TOXIC LIKE, WHEN REMOVING IT IS CAUSING BRUISING AND OR SKIN TEARS TO PATIENTS. THE SKIN DISCOLORATION IS NOTICED IMMEDIATELY AFTER REMOVING. SIMILAR EVENT ALSO HAPPENED IN THE FALL.

  Patient problems: Bruise/Contusion; Skin Discoloration

  MAUDE report 12967486 ↗