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Jet-X 71067376Recalls & reported problems

Smith & Nephew, Inc. · JET-X 6 HOLE PIN CLAMP · Class 2 · Implant

Data updated Oct 13, 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 03596010607898), received between Jun 19, 2019 and Jun 19, 2019 — classified as 1 malfunction.

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

  • Break1

Patient problems

  • No Consequences Or Impact To Patient1

Recent adverse event reports

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

  • MalfunctionJun 19, 2019Break; Break

    IT WAS REPORTED THAT WHILE TIGHTENING JET-X CLAMP, IT BROKE. DELAY OF ONE MINUTE REPORTED. BACKUP DEVICE AVAILABLE. NO INJURY OR IMPACT TO PATIENT.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8712938 ↗

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Sources and updates

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