VARIAX 657326SRecalls & reported problems
Stryker GmbH · Locking Screw · Class 2 · Implant
All models of VARIAX (345)
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 07613327087024), received between Oct 26, 2021 and Dec 22, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Material Fragmentation” (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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Material Fragmentation1
- Positioning Failure1
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.
MalfunctionDec 22, 2023Material Fragmentation; Material Fragmentation
AS REPORTED: "THREADED PIECES OF METAL APPEARED WHEN TIGHTENING A SCREW TO THE PLATE."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18389237 ↗MalfunctionOct 26, 2021Positioning Failure; Positioning Failure
IT WAS REPORTED A LOCKING FAILURE OCCURRED. IT IS POSSIBLE THAT THE ALLOWABLE ANGLE OF LOCKING HAS BEEN EXCEEDED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12699085 ↗
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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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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