Valor® 415101020LRecalls & 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
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00840420125507), received between Feb 14, 2022 and Feb 10, 2025 — classified as 2 injuries.
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
- Fracture1
- Migration1
Patient problems
- Inflammation1
- Insufficient Information1
- Nonunion/Delayed-union Bone Fracture1
- Unspecified Infection1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryFeb 10, 2025Break; Fracture; Break; Fracture
ITALIAN DISTRIBUTOR WALDNER REPORTED THAT A VALOR NAIL WAS REMOVED IN ABANO ON WEDNESDAY 8TH. THE NAIL BROKE 7 YEARS AFTER IMPLANTATION. THE BREAK POINT CORRESPONDS TO THE HOLE FOR THE SUBTALAR SCREW THAT HAD NOT BEEN PLACED. UNANTICIPATED MEDICAL PROCEDURE.
Patient problems: Insufficient Information
MAUDE report 21342989 ↗InjuryFeb 14, 2022Migration; Migration
IT WAS REPORTED THAT THE IM NAIL LOOSENED AND CAUSED INFECTION THAT LED TO A NONUNION OF THE ANKLE FUSION SITE. IT REQUIRED REMOVAL OF THE IM NAIL WITH BONE BIOPSIES AND PLACEMENT OF ANTIBIOTIC CEMENT NAIL WITH IV ANTIBIOTICS FOLLOWED BY REVISION OF ANKLE FUSION WITH EXTERNAL FIXATOR.
Patient problems: Inflammation; Nonunion/Delayed-union Bone Fracture; Unspecified Infection
MAUDE report 13523826 ↗
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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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