CERVICAL TRACTION VECTOR ADJUSTER 7803-790Recalls & reported problems

Summary

The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 00842430111679), received between Apr 1, 2021 and Apr 4, 2023 — classified as 3 malfunctions.

The most frequently reported specific device problem is “Device Dislodged or Dislocated” (2 reports).

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 16, 2026.

Most reported problems

Recent adverse event reports

The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 4, 2023Device Slipped; Device Slipped

  PATIENT WAS HAVING A POSTERIOR CERVICAL FUSION USING GARDNER WELLS TONGS AND TRIOS VECTOR TRACTION. TRIOS VECTOR TRACTION SLIPPED MID CASE AND PATIENTS HEAD FELL AND WAS CAUGHT BY THE HORSESHOE HEADREST. PATIENT WAS NOT INJURED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 16677760 ↗
• MalfunctionApr 27, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated

  IT WAS REPORTED A BRAND-NEW TRACTION VECTOR CONNECTED TO 15 LBS OF WEIGHT AND GW TONGS ATTACHED TO PATIENT'S HEAD POPPED OFF UPPER TOWER OF TRIOS TABLE DURING A POST CERVICAL PROCEDURE.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11733719 ↗
• MalfunctionApr 1, 2021Device Dislodged or Dislocated; Device Dislodged or Dislocated

  CUSTOMER REPORTED THAT TRACTION VECTOR POPPED OFF TOWER IN THE MIDDLE OF A CERVICAL CASE. THE SURGEON APPLIED THE VECTOR HIMSELF AND USES THIS ATTACHMENT FREQUENTLY. THE PATIENT WAS NOT INJURED.

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 11602149 ↗