A.L.P.S. mvX™ 770714102Recalls & reported problems
Tyber Medical, LLC · ANTLATERAL TIB PLT 10H RT WIDE · Class 2 · Implant
All models of A.L.P.S. mvX (25)
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 00196449015900), received between Dec 31, 2024 and Dec 31, 2024 — classified as 1 malfunction.
The most frequently reported specific device problem is “Difficult or Delayed Positioning” (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
- Difficult or Delayed Positioning1
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.
MalfunctionDec 31, 2024Difficult or Delayed Positioning; Difficult or Delayed Positioning
SURGEON TRIED PUTTING IN SCREW INTO OBLONG HOLE TOWARDS TOP OF THE ANTEROLATERAL DISTAL TIBIA PLATE AND SCREW HEAD BROKE OFF FAIRLY EASILY. HE THEN PUT A SCREW IN JUST PROXIMAL TO THE FIRST AND SCREW HEAD PASSED THROUGH THE PLATE AND WAS STUCK UNDER PLATE. 2-HOUR SURGICAL DELAY NOTED AFTER SURGEON TRIED TO REMOVE BROKEN SCREW AND THE SCREW UNDER THE PLATE. SCREW WAS DISCARDED AND PLATE WAS RETAINED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21049118 ↗
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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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