Medline DYNJP7002Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10080196736508), received between Mar 17, 2021 and Sep 12, 2026 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Adhesive Too Strong” (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 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionSep 12, 2026Adhesive Too Strong

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50746511 ↗
• MalfunctionSep 3, 2026Material Split, Cut or Torn

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50587593 ↗
• MalfunctionMar 17, 2021Contamination

  UPON CLOSING COUNT THE NURSE DISCOVERED A SINGLE STRAND OF HAIR CLINGING TO ONE OF THE STERILE LAP SPONGES OF MEDLINE THYROID SURGICAL DRAPE. ALL STAFF INCLUDING PATIENT WERE WEARING A HAIR COVERING.

  Patient problems: Insufficient Information

  MAUDE report 11504467 ↗