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JET-X 71063027Recalls & reported problems

Smith & Nephew, Inc. · JETX DRILL SLEEVE W/TROCAR F/5 & 6MM SHORT HP · Class 1

All models of Jet-X (24)

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
2
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00885556013687), received between Aug 22, 2019 and Aug 12, 2021 — classified as 2 malfunctions.

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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Break1
  • Defective Component1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1
  • No Consequences Or Impact To Patient1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • MalfunctionAug 12, 2021Break; Break

    (B)(6). IT WAS REPORTED THAT, DURING AN JETX SURGERY, ONE JETX DS/TROC F/5 & 6MM SHT HP WAS BROKEN WHEN TRYING TO CHANGE THE CENTERING SLEEVE. SURGERY WAS RESUMED, WITHOUT ANY DELAY. NO HEALTH CONSEQUENCES WERE REPORTED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 12314511 ↗
  • MalfunctionAug 22, 2019Defective Component; Defective Component

    IT WAS REPORTED THAT, DURING DRILLING, IT WAS FOUND DAMAGED. BACKUP DEVICE WAS AVAILABLE AND THE SURGERY DELAYED 1 HOUR.

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 8920342 ↗

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Sources and updates

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