ANTHEM 2168.2103Recalls & reported problems
Globus Medical, Inc. · ANTHEM Proximal Humerus Plate, Right, 103mm, SS · Class 2
All models of ANTHEM (27)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00889095639346), received between Mar 5, 2024 and Mar 5, 2024 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Fracture” (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
- Fracture1
- Mechanical Problem1
Patient problems
- Insufficient Information1
- Spinal Column Injury1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionMar 5, 2024Mechanical Problem; Mechanical Problem
THERE WAS A REVISION TO REPLACE AN ANTHEM PROXIMAL HUMERUS PLATE THAT WAS FOUND BROKEN POST OPERATIVELY.
Patient problems: Spinal Column Injury
MAUDE report 18837912 ↗MalfunctionMar 5, 2024Fracture; Fracture
IT WAS REPORTED THAT A REVISION WAS NEEDED TO REPLACE AN ANTHEM PROXIMAL HUMERUS PLATE THAT WAS BROKEN 2 WEEKS POST OPERATIVELY.
Patient problems: Insufficient Information
MAUDE report 18834291 ↗
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- PRECICE® Plating System LP4.5-PLF4BNuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls3 reports
- PRECICE® Plating System LP4.5-MRT4BNuvasive 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-PLF40Nuvasive Specialized Orthopedics, Inc. · Plate, Fixation, Bone3 recalls0 reports
- PRECICE® Plating System LP4.5-PRT42Nuvasive 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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