VG2 273350106Recalls & reported problems

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10705034189154), received between Feb 12, 2020 and Mar 4, 2024 — classified as 2 malfunctions.

The most frequently reported specific device problem is “Break” (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 18, 2026.

Most reported problems

Recent adverse event reports

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

• MalfunctionMar 4, 2024Break; Crack; Break; Crack

  IT WAS REPORTED THAT ON (B)(6) 2024, THE STERILE PROCESSING DEPARTMENT NOTIFIED OF CRACKED/BROKEN INSTRUMENTS THAT COULD NOT BE PROCESSED DUE TO STERILIZATION RULES AND PROCESS. ISSUES WERE NOTED POSTOPERATIVELY. THERE WAS NO PATIENT CONSEQUENCE. THIS REPORT INVOLVES ONE VG2 CERVICAL INSTRUMENTS TRIAL 4 X 6MM. THIS IS REPORT 1 OF 10 FOR (B)(4).

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 18826954 ↗
• MalfunctionFeb 12, 2020Break; Break

  LIBERTAS: IT WAS REPORTED THAT ON NOVEMBER 13, 2019, THE EXP 635/635 CLS/CLS SDXSD CON WAS FOUND TO BE BROKEN DURING REVERSE LOGISTICS AUDIT OF RETURNED DEVICE AT (B)(6). THERE WAS NO PATIENT INVOLVEMENT AND NO ADDITIONAL INFORMATION IS AVAILABLE. THIS COMPLAINT INVOLVES ONE (1) VG2 CERVICAL TRIAL STAND 4X6. THIS REPORT IS 1 OF 1 FOR (B)(4).

  Patient problems: No Patient Involvement

  MAUDE report 9702099 ↗