Valor® 415101015LRecalls & reported problems
Wright Medical Technology, Inc. · Class 2 · Implant
All models of VALOR (25)
Data updated Oct 18, 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 00840420125484), received between May 14, 2021 and Feb 22, 2022 — 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 18, 2026.
Most reported problems
Device problems
- Adverse Event Without Identified Device or Use Problem1
- Break1
Patient problems
- Bacterial Infection1
- Pain1
- 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 22, 2022Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
IT WAS REPORTED VIA A PRODUCT LIABILITY CLAIM THAT THE PATIENT HAD AN ANKLE NAIL AND SCREWS IMPLANTED. SOMETIME POST-OP THE PATIENT UNDERWENT A REVISION DUE TO AN INFECTION. THE PATIENT APPARENTLY HAD AN AMPUTATION DUE TO THE INFECTION.
Patient problems: Bacterial Infection; Unspecified Infection
MAUDE report 13581744 ↗InjuryMay 14, 2021Break; Break
IT WAS REPORTED THAT THE PATIENT HAD PAIN SOMETIME POST-OP AND WENT TO SEE THE SURGEON. IT WAS FOUND THAT THE NAIL HAD SNAPPED IN HALF. THE PATIENT UNDERWENT A REVISION SURGERY.
Patient problems: Pain
MAUDE report 11824701 ↗
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- HEALIX PEEK ORTHOCORD 222205Medos International Sàrl · Screw, fixation, bone186 reports
- PRECICE® Bone Transport System STP3.5-400Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-225Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-350Nuvasive Specialized Orthopedics, Inc. · Screw, Fixation, Bone3 recalls0 reports
- PRECICE® Bone Transport System STP3.5-300Nuvasive 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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