ORTHOLOC 3DI 52020304Recalls & reported problems
Wright Medical Technology, Inc. · Small Bones · Class 2 · Implant
All models of ORTHOLOC 3Di (23)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00840420185426), received between Sep 29, 2023 and Sep 29, 2023 — classified as 1 injury.
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
- Break1
- Fracture1
Patient problems
- Failure of Implant1
- Implant Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjurySep 29, 2023Break; Fracture; Break; Fracture
A PATIENT UNDERWENT SURGERY DURING WHICH A SMALL BONES STRAIGHT PLATE (52020304) WAS IMPLANTED. SUBSEQUENTLY, THE PLATE BROKE, AS CONFIRMED BY AN IN-CLINIC X-RAY. THE PATIENT APPROACHED THE PHYSICIAN REGARDING A POTENTIAL ISSUE WITH THE PRODUCT, AND THE PHYSICIAN SAW THE PATIENT FOR FURTHER EVALUATION. THE PHYSICIAN BELIEVES THE PATIENT WAS COMPLIANT WITH MOBILIZATION INSTRUCTIONS. THE PATIENT NOTICED THE EVENT DUE TO FOOT PAIN AND SOUGHT AN X-RAY, BUT THE EXACT DATE IS UNCERTAIN. THE IMPLANT WAS INITIALLY USED FOR A NON-DISPLACED 5TH METATARSAL BASE FRACTURE (AO CLASSIFICATION). THE EVENT IS CURRENTLY BEING MANAGED WITHOUT A REVISION PROCEDURE, AND THE PATIENT IS USING A BONE STIMULATOR.
Patient problems: Failure of Implant; Implant Pain
MAUDE report 17848642 ↗
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- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-DRF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls1 report
- PRECICE® Plating System LP4.5-MLT42Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-MRT42Nuvasive Specialized Orthopedics, Inc. · Plate, 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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