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MatrixRIB 03.501.033Recalls & reported problems

Synthes GmbH · 2.2MM THREADED DRILL GUIDE FOR MATRIXRIB LOCKING PLATES · Class 1

All models of MatrixRIB (31)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
11
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 11 adverse event reports that list this exact device (DI 10887587010649), received between Aug 24, 2018 and Apr 2, 2026 — classified as 11 malfunctions.

The most frequently reported specific device problem is “Material Deformation” (5 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 16, 2026.

Reports received per month

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 1 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 1 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520261
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Material Deformation5
  • Material Twisted/Bent5
  • Break1
  • Device-Device Incompatibility1

Patient problems

  • No Clinical Signs, Symptoms or Conditions7
  • No Consequences Or Impact To Patient2
  • No Patient Involvement1
  • Not Applicable1

Recent adverse event reports

The 11 most recent of 11 reports, in the reporter's own words as published by the FDA.

  • MalfunctionApr 2, 2026Material Deformation

    IT WAS REPORTED THAT THE 2.2 THRD DRILL GUIDE MATRIXRIB LCKNG PLS WAS BENT DURING ROUTINE TESTING OF FIELD EQUIPMENT. THE EVENT INVOLVED NO ACCOUNT OR PATIENT PARTICIPATION, AND THERE WAS NO REPORTED PATIENT OR USER HARM OR SIGNIFICANT DELAY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24768358 ↗
  • MalfunctionMar 5, 2024Break; Break

    IT WAS REPORTED THAT ON 19-FEBRUARY-2024, THE COLLAR OF THE PRODUCT IN QUESTION BROKE OFF. THERE WERE NO PATIENT CONSEQUENCES. NO FURTHER INFORMATION IS AVAILABLE. THIS REPORT IS FOR A 2.2MM THREADED DRILL GUIDE FOR MATRIXRIB LOCKING PLATES. THIS IS REPORT 1 OF 1 FOR (B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 18835977 ↗
  • MalfunctionSep 18, 2023Device-Device Incompatibility; Material Twisted/Bent; Device-Device Incompatibility; Material Twisted/Bent

    DEVICE REPORT FROM DEPUY SYNTHES REPORTS AN EVENT IN (B)(6) AS FOLLOWS: IT WAS REPORTED THAT THE GUIDE WAS TWISTED DURING THE SURGERY ON (B)(6) 2023, WHICH MAKES IT DIFFICULT TO PASS THE DRILL BIT. THERE WAS NO PATIENT IMPACT. THIS REPORT IS FOR ONE (1) 2.2MM THREADED DRILL GUIDE FOR MATRIXRIB LOCKING PLATES. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 17766001 ↗
  • MalfunctionJan 9, 2023Material Deformation; Material Deformation

    THERE WAS NO SURGICAL DELAY. THE PROCEDURE WAS SUCCESSFULLY COMPLETED.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16126262 ↗
  • MalfunctionDec 19, 2022Material Deformation; Material Deformation

    DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN COLOMBIA AS FOLLOWS: IT WAS REPORTED ON (B)(6) 2022, THAT THE DRILL GUIDE WAS CROOKED AFTER SURGERY. IT DID NOT THREAD WELL INTO THE HOLE IN THE PLATE. CONCOMITANT DEVICE REPORTED: UNK - PLATES: TRAUMA (PART# UNKNOWN; LOT# UNKNOWN; QUANTITY: UNKNOWN). THIS REPORT IS FOR ONE (1) MATRIXRIB DRILL GUID 2.2 F/PL. THIS IS REPORT 1 OF 1 FOR COMPLAINT (B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 16005829 ↗
  • MalfunctionNov 15, 2022Material Deformation; Material Deformation

    DEVICE REPORT FROM SYNTHES REPORTS AN EVENT IN COLOMBIA AS FOLLOWS: IT WAS REPORTED THAT DURING A PROCEDURE ON (B)(6) 2022, THE MATRIX RIBS 2.2 DRILL GUIDE WAS FOUND TO BE BENT ON THE THREADED PART. THE INTERVENTION WAS SUCCESSFULLY COMPLETED, AND THERE WAS NO DELAY DUE TO THE REPORTED EVENT. THE PATIENT OUTCOME WAS SATISFACTORY AT THE END OF THE PROCEDURE. THIS REPORT INVOLVES ONE 2.2MM THREADED DRILL GUIDE FOR MATRIXRIB LOCKING PLATES. THIS IS REPORT 1 OF 1 FOR (B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15796601 ↗
  • MalfunctionOct 5, 2022Material Deformation; Material Deformation

    IT WAS REPORTED THAT ON (B)(6) 2022, THE DRILL GUIDE WAS BENT. THIS REPORT INVOLVES ONE 2.2MM THREADED DRILL GUIDE FOR MATRIXRIB LOCKING PLATES. THIS IS REPORT 1 OF 1 FOR (B)(4).

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15544785 ↗
  • MalfunctionOct 29, 2019Material Twisted/Bent; Material Twisted/Bent

    CONCOMITANT DEVICE: UNKNOWN PLATE (PART# UNKNOWN, LOT# UNKNOWN, QUANTITY# 1).

    Patient problems: Not Applicable

    MAUDE report 9251955 ↗
  • MalfunctionOct 17, 2018Material Twisted/Bent; Material Twisted/Bent

    IT WAS REPORTED THAT THE THREADED DRILL GUIDE WAS DISCOVERED TO HAVE STRIPPED OUT WHILE THE SURGEON ATTEMPTED TO SCREW IN THE THREADED DRILL GUIDE TO THE MATRIXRIB LOCKING PLATE, DURING A THORACIC PROCEDURE ON AN UNKNOWN DATE. THE PROCEDURE WAS SUCCESSFULLY COMPLETED USING THE DRILL SLEEVES IN THE SET. IT WAS UNKNOWN IF THERE WAS A SURGICAL DELAY. PATIENT OUTCOME WAS UNKNOWN. CONCOMITANT DEVICE REPORTED: MATRIXRIB PLATE (PART # UNKNOWN, LOT # UNKNOWN, QUANTITY UNKNOWN). THIS REPORT IS FOR ONE (1) 2.2MM THREADED DRILL GUIDE FOR MATRIXRIB LOCKING PLATES. THIS IS REPORT 2 OF 2 FOR COMPLAINT (B)(4).

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7973866 ↗
  • MalfunctionOct 17, 2018Material Twisted/Bent; Material Twisted/Bent

    IT WAS REPORTED THAT THE THREADED DRILL GUIDE WAS DISCOVERED TO HAVE STRIPPED OUT WHILE THE SURGEON ATTEMPTED TO SCREW IN THE THREADED DRILL GUIDE TO THE MATRIXRIB LOCKING PLATE, DURING A THORACIC PROCEDURE ON AN UNKNOWN DATE. THE PROCEDURE WAS SUCCESSFULLY COMPLETED USING THE DRILL SLEEVES IN THE SET. IT WAS UNKNOWN IF THERE WAS A SURGICAL DELAY. PATIENT OUTCOME WAS UNKNOWN. CONCOMITANT DEVICE REPORTED: MATRIXRIB PLATE (PART # UNKNOWN, LOT # UNKNOWN, QUANTITY UNKNOWN). THIS REPORT IS FOR ONE (1) 2.2MM THREADED DRILL GUIDE FOR MATRIXRIB LOCKING PLATES. THIS IS REPORT 1 OF 2 FOR COMPLAINT (B)(4).

    Patient problems: No Consequences Or Impact To Patient

    MAUDE report 7973823 ↗
  • MalfunctionAug 24, 2018Material Twisted/Bent; Material Twisted/Bent

    (B)(6) REPORTS THAT THE TIP OF THE THREADED DRILL GUIDE FOR MATRIXRIB LOCKING PLATES WAS FOUND OUT TO BE BENT, AND THEREFORE UNUSABLE, UPON DELIVERING AN IN-SERVICE TO MEDICAL DEVICE REPROCESSING DELIVERY (MDRD). THERE WAS NO PATIENT INVOLVEMENT. THIS REPORT IS FOR A 2.2MM THREADED DRILL GUIDE FOR MATRIXRIB LOCKING PLATES. THIS IS REPORT 1 OF 1 FOR (B)(4).

    Patient problems: No Patient Involvement

    MAUDE report 7814067 ↗

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