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NA 72201551Recalls & reported problems

Smith & Nephew, Inc. · MEDIUM/LARGE WRIST STABILIZATION KITS, DISPOSABLE 5 PER CASE · Class 1

Data updated Oct 13, 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 03596010604972), received between Aug 31, 2023 and Aug 31, 2023 — classified as 1 injury.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (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. How this data works · Data updated Oct 13, 2026.

Most reported problems

Device problems

  • Insufficient Device Problem Information1

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.

  • InjuryAug 31, 2023Insufficient Device Problem Information; Insufficient Device Problem Information

    IT WAS REPORTED THAT DURING A WRIST ARTHROSCOPY PROCEDURE, UNSPECIFIED FLAWS WERE NOTED ON THE INCISOR PLUS. THE PROCEDURE WAS SUCCESSFULLY COMPLETED WITH NO SURGICAL DELAY, APPLYING A CHANGE IN THE SURGICAL TECHNIQUE, AN OPEN SURGERY WAS PERFORMED. NO FURTHER COMPLICATIONS WERE REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17663348 ↗

Other Accessories, operating-room, table (kit) devices

All Accessories, operating-room, table (kit) devices →

Sources and updates

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