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NA 72200488Recalls & reported problems

Smith & Nephew, Inc. · SPIDER INDEXING HANDLE REPLACEMENT KIT · Class 1

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 03596010551726), received between Dec 23, 2020 and Dec 23, 2020 — classified as 1 malfunction.

The most frequently reported specific device problem is “Physical Resistance/Sticking” (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

  • Physical Resistance/Sticking1

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.

  • MalfunctionDec 23, 2020Physical Resistance/Sticking; Physical Resistance/Sticking

    IT WAS REPORTED THAT, DURING SET UP, THE HANDLE THAT TIGHTENS THE SPIDER ARM POSITIONER TO THE BED STRIPPED INTERNALLY AND THE STAFF WAS NO LONGER ABLE TO TIGHTEN OR LOOSEN THE DEVICE. NO DELAYS OR PATIENT INVOLVEMENT WERE REPORTED. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL REPORT WILL BE SUBMITTED ACCORDINGLY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 11070375 ↗

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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.