Valor® 415101020RRecalls & reported problems
Wright Medical Technology, Inc. · Class 2 · Implant
All models of VALOR (25)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00840420125514), received between May 26, 2021 and Aug 21, 2025 — classified as 1 injury, 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 16, 2026.
Reports received per month
Most reported problems
Device problems
- Break1
- Failure to Advance1
- Fracture1
Patient problems
- Failure of Implant1
- Insufficient Information1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryAug 21, 2025Break; Fracture; Break; Fracture
AS REPORTED: "ORIGINAL SURGERY WAS (B)(6) 2024. AT SOME POINT MONTHS AFTER, THE NAIL BROKE".
Patient problems: Insufficient Information
MAUDE report 22864660 ↗MalfunctionMay 26, 2021Failure to Advance; Failure to Advance
IT WAS REPORTED THAT THE INTERNAL COMPRESSION SCREW COULD NOT BE TURNED AND REMOVED. THE SURGEON REMOVED THE IMPLANT AND INSERTED A NEW IMPLANT WHICH EXTENDED THE SURGERY TIME AS WELL AS TOURNIQUET TIME AND EXTRA HOLES IN THE BONE. NO ADDITIONAL PATIENT COMPLICATIONS WERE REPORTED.
Patient problems: Failure of Implant
MAUDE report 11889290 ↗
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- HEALIX PEEK ORTHOCORD 222205Medos International Sàrl · Screw, fixation, bone186 reports
- PRECICE® Bone Transport System STP3.5-350Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-400Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-300Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-200Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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