VG2 273350110Recalls & reported problems
Medos International Sàrl · VG2 CERVICAL INSTRUMENTS TRIAL, STANDARD 8 x 10mm · Class 1
Data updated Oct 18, 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 10705034189192), received between Mar 4, 2024 and Mar 4, 2024 — 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. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.
Reports received per month
Most reported problems
Device problems
- Appropriate Device Problem Term/Code Not Available1
- Break1
- Crack1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 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 (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, STANDARD 8 X 10MM. THIS IS REPORT 5 OF 10 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18826956 ↗
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- DELTA XTEND 2307-95-000Depuy (Ireland) · TEMPLATE315 reports
- ATTUNE 2545-00-547Depuy (Ireland) · TEMPLATE1 recall231 reports
- ATTUNE 2544-00-520Depuy (Ireland) · TEMPLATE279 reports
- ATTUNE 2545-00-545Depuy (Ireland) · TEMPLATE1 recall221 reports
- ARTICUL/EZE 2530-91-000Depuy (Ireland) · TEMPLATE271 reports
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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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