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NA 72201428Recalls & reported problems

Smith & Nephew, Inc. · SPIDER LATERAL JACK · 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 03596010651310), received between Apr 14, 2021 and Apr 14, 2021 — classified as 1 malfunction.

The most frequently reported specific device problem is “Unstable” (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

  • Unstable1

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.

  • MalfunctionApr 14, 2021Unstable; Unstable

    IT WAS REPORTED THAT THE SHOULDER DIST LATERAL JACK SPIDER WAS NOT WORKING. NO CASE INVOLVED. RESULTS OF INVESTIGATION HAVE CONCLUDED THAT THE BLUE ROTATIONAL HANDLE WOULD NOT FULLY LOCK DOWN TO SECURE THE PAD ASSEMBLY SHAFT WHICH MAKES IT A REPORTABLE. 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 11664631 ↗

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