MatrixRIB 04.501.095Recalls & reported problems
Synthes GmbH · TI MATRIXRIB STRAIGHT PLATE 2.8MM THICK/10 HOLES · Class 2 · Implant
All models of MatrixRIB (31)
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 10887587072371), received between Jun 16, 2025 and Jun 16, 2025 — classified as 1 injury.
The most frequently reported specific device problem is “Migration” (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.
Reports received per month
Most reported problems
Device problems
- Migration1
Patient problems
- Pain1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJun 16, 2025Migration; Migration
IT WAS REPORTED REVISION SURGERY OCCURRED ON (B)(6) 2025 DUE TO DEVICE MIGRATION AND PATIENT REPORT OF PAIN. THE SURGEON ORIGINALLY PLATED PATIENT'S 7TH RIB ON (B)(6) 2024 WITH STERNAL PLATE FOR SURGICAL STABILIZATION OF RIB FRACTURE. DURING THE REVISION, THE SURGEON HAD TO REMOVE THE PLATE AS THE PLATE AND SCREWS WERE BACKING OUT OF THE BONE AND COMING AWAY FROM THE RIB. MEDIAL SCREWS WERE REMOVED WITH A DRIVER WHILE THE LATERAL SCREWS JUST PULLED OUT OF THE BONE. THE SURGEON BELIEVES IT IS DUE TO UNDER CONTOURING OF THE PLATE. IT WAS NOTED THE SURGEON WAS FOLLOWING THE CORRECT SURGICAL TECHNIQUE IN THE ORIGINAL SURGERY. IT WAS FURTHER MENTIONED IT WAS NOT CLEAR IF THE PATIENT HAD BEEN COMPLIANT POST INITIAL PROCEDURE. THERE WAS CALLUS NOTED IN THE BONE DURING THE REVISION SO NO FURTHER DEVICES WERE IMPLANTED.
Patient problems: Pain
MAUDE report 22211385 ↗
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- 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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