MatrixRIB 03.501.703Recalls & reported problems
Synthes GmbH · TROCAR FOR MATRIXRIB SYSTEM · Class 1
All models of MatrixRIB (31)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10887587011363), received between Aug 4, 2021 and Aug 4, 2021 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Material Deformation” (2 reports).
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
- Material Deformation2
- Corroded1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 4, 2021Material Deformation; Material Deformation
DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN (B)(6) AS FOLLOWS: IT WAS REPORTED THAT THE THREE INSTRUMENTS WERE DISCOVERED TO HAVE SMALL HOLES AND MARKINGS ON THE HANDLES. NO SURGICAL OR PATIENT INVOLVEMENT. THIS REPORT IS FOR (1) TROCAR FOR MATRIXRIB SYSTEM. THIS IS REPORT 3 OF 3 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12273556 ↗MalfunctionAug 4, 2021Material Deformation; Material Deformation
DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN (B)(6) AS FOLLOWS: IT WAS REPORTED THAT THE THREE INSTRUMENTS WERE DISCOVERED TO HAVE SMALL HOLES AND MARKINGS ON THE HANDLES. NO SURGICAL OR PATIENT INVOLVEMENT. THIS REPORT IS FOR ONE (1) TROCAR FOR MATRIXRIB SYSTEM. THIS IS REPORT 2 OF 3 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12273554 ↗MalfunctionAug 4, 2021Corroded; Corroded
DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN (B)(6) AS FOLLOWS: IT WAS REPORTED THAT THE THREE INSTRUMENTS WERE DISCOVERED TO HAVE SMALL HOLES AND MARKINGS ON THE HANDLES. NO SURGICAL OR PATIENT INVOLVEMENT. THIS REPORT IS FOR (1) TROCAR FOR MATRIXRIB SYSTEM. THIS IS REPORT 1 OF 3 FOR (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12273553 ↗
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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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