Virage® 07.01702.023Recalls & reported problems
Zimmer Biomet Inc · Class 2
All models of Virage (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 00889024327160), received between Jun 25, 2024 and Jun 25, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fracture” (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.
Reports received per month
Most reported problems
Device problems
- Fracture2
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 25, 2024Fracture; Fracture
IT WAS REPORTED THAT DURING FINAL TIGHTENING OF A C4/C7 FIXATION, AN ABNORMAL SOUND WAS OBSERVED, AND FOUND THAT TWO VIRAGE SCREWS' HOUSINGS WERE FRACTURED AT THE WELDS. THERE WAS A 30-MINUTE DELAY TO REMOVE THE BROKEN SCREWS AND REPLACE THEM WITH NEW SCREWS. THERE WAS NO IMPACT ON THE PATIENT. THIS IS REPORT TWO OF TWO FOR THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19606522 ↗MalfunctionJun 25, 2024Fracture; Fracture
IT WAS REPORTED THAT DURING FINAL TIGHTENING OF A C4/C7 FIXATION, AN ABNORMAL SOUND WAS OBSERVED, AND FOUND THAT TWO VIRAGE SCREWS' HOUSINGS WERE FRACTURED AT THE WELDS. THERE WAS A 30-MINUTE DELAY TO REMOVE THE BROKEN SCREWS AND REPLACE THEM WITH NEW SCREWS. THERE WAS NO IMPACT ON THE PATIENT. THIS IS REPORT ONE OF TWO FOR THIS EVENT.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 19606506 ↗
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- EXPEDIUM VIPER 196789480Depuy Spine, LLC · APPLIANCE, FIXATION, SPINAL INTERLAMINAL72 reports
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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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