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Opsite Post-Op Visible 30x10cm Ctn 20 66800140Recalls & reported problems

Smith & Nephew Medical Limited · Waterproof, bacteria proof dressing with absorbent see through pad · Class 1

Data updated Oct 18, 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 05000223468620), received between Sep 8, 2021 and Sep 8, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Patient-Device Incompatibility” (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 18, 2026.

Most reported problems

Device problems

  • Adverse Event Without Identified Device or Use Problem1
  • Patient-Device Incompatibility1

Patient problems

  • Skin Discoloration1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 8, 2021Patient-Device Incompatibility; Adverse Event Without Identified Device or Use Problem; Patient-Device Incompatibility; Adverse Event Without Identified Device or Use Problem

    IT WAS REPORTED THAT A STERILE WOUND DRESSING (OPSITE POST-OP VISIBLE) WAS APPLIED AFTER A HIP ARTHROPLASTY ON THE RIGHT THIGH. AT FOLLOW-UP 3 MONTHS POST-OP, A SHADING ON THE SKIN ACCORDING TO THE HONEYCOMB PATTERN OF THE DRESSING IS NOTICEABLE AND IT'S QUESTIONABLE IF THIS ADVERSE EVENT IS REVERSIBLE. NO MEDICAL INTERVENTION WAS REQUIRED.

    Patient problems: Skin Discoloration

    MAUDE report 12443099 ↗

Other Tape And Bandage, Adhesive devices

All Tape And Bandage, Adhesive devices →

Sources and updates

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