VG2 273340107Recalls & reported problems
Medos International Sàrl · VG2 CERVICAL INSTRUMENTS RASP/TRIAL 7mm · Class 1
Data updated Oct 16, 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 10705034189055), received between Oct 25, 2019 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break2
- Appropriate Device Problem Term/Code Not Available1
- Crack1
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.
MalfunctionMar 4, 2024Break; Crack; Appropriate Device Problem Term/Code Not Available; Break; Crack; Appropriate Device Problem Term/Code Not Available
IT WAS REPORTED THAT ON FEBRUARY 16, 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 RASP/TRIAL 7MM. THIS IS REPORT 7 OF 10 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18826964 ↗MalfunctionOct 25, 2019Break; Break
LIBERTAS: IT WAS REPORTED THAT ON (B)(6) 2019, THE 6MM DUAL-LEAD TAP WAS FOUND TO BE BROKEN DURING REVERSE LOGISTICS AUDIT OF RETURNED DEVICE AT MILLSTONE. THERE WAS NO PATIENT INVOLVEMENT AND NO ADDITIONAL INFORMATION IS AVAILABLE. THIS COMPLAINT INVOLVES ONE (1) DEVICE.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 9240796 ↗
Other RASP, SURGICAL, GENERAL & PLASTIC SURGERY devices
- Progressive proximal rasp PIP 211-A43000Keri Medical SA · Rasp, Surgical, General & Plastic Surgery4 reports
- VG2 273340106Medos International Sàrl · RASP, SURGICAL, GENERAL & PLASTIC SURGERY2 reports
- NA 698273327Depuy Spine, LLC · RASP, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- VG2 273340108Medos International Sàrl · RASP, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- CONCORDE 287903001Depuy Spine, LLC · RASP, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- CONCORDE 287903003Depuy Spine, LLC · RASP, SURGICAL, GENERAL & PLASTIC SURGERY1 report
- Innomed, Inc. 3004-01Innomed, Inc. · Rasp, Surgical, General & Plastic Surgery1 report
- VG2 273340109Medos International Sàrl · RASP, SURGICAL, GENERAL & PLASTIC SURGERY1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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