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Opsite Post-Op Visible 35x10cm Ctn 20 66800141Recalls & 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
1
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 05000223468637), received between Jan 12, 2021 and Jan 12, 2021 — classified as 1 injury.

The most frequently reported specific device problem is “Packaging Problem” (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

  • Packaging Problem1

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.

  • InjuryJan 12, 2021Packaging Problem; Packaging Problem

    IT WAS REPORTED THAT DURING SET UP THE PACKAGE WAS FOUND DEFECTIVE. IT IS UNKNOWN WHAT HAPPENED TO THE PACKAGE. TREATMENT WAS STARTED WITH THE COMPETITORS PRODUCT. NO PATIENT HARM WAS REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11157082 ↗

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Sources and updates

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