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Matrix 03.511.340Recalls & reported problems

Synthes GmbH · MATRIX 1.4MM DRILL BIT/J-LATCH CALIBRATED FOR 03.511.009 · Class 2

All models of Matrix (80)

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

Adverse event reports
2
Deaths reported
0
Injuries reported
2
Recalls naming it
0

Summary

The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 10887587014425), received between Jul 26, 2021 and Dec 1, 2022 — classified as 2 injuries.

The most frequently reported specific device problem is “Entrapment of Device” (1 report).

6 other recalls cover devices cleared under the same FDA submission (K043310); they may or may not involve this specific model.

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.

Most reported problems

Device problems

  • Entrapment of Device1
  • Overheating of Device1

Patient problems

  • Burn(s)1
  • Foreign Body In Patient1
  • Unspecified Tissue Injury1

Recent adverse event reports

The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.

  • InjuryDec 1, 2022Overheating of Device; Overheating of Device

    IT WAS REPORTED THAT ON (B)(6) 2022 DURING SURGERY, THE DRILL BIT GOT UNUSUALLY HOT AND BURNED THE BONE. THE SURGERY WAS COMPLETED SUCCESSFULLY AFTER CHANGING THE DRILL BIT. NO FURTHER INFORMATION IS AVAILABLE. THIS REPORT INVOLVES ONE MATRIX 1.4MM DRILL BIT/J-LATCH CALIBRATED FOR 03.511.009. THIS IS REPORT 1 OF 1 FOR (B)(4).

    Patient problems: Burn(s); Unspecified Tissue Injury

    MAUDE report 15895958 ↗
  • InjuryJul 26, 2021Entrapment of Device; Entrapment of Device

    IT WAS REPORTED THAT ON (B)(6) 2021, THE SURGEON WAS NOTIFIED THAT HE HAD TO DO A REVISION TO RETRIEVE A DRILL BIT. NO SURGICAL DELAY. THE PROCEDURE SUCCESSFULLY COMPLETED. THE PATIENT OUTCOME IS UNKNOWN. THIS REPORT IS FOR A DRILL BIT. THIS IS REPORT 1 OF 1 FOR (B)(4).

    Patient problems: Foreign Body In Patient

    MAUDE report 12224852 ↗

Recalls under the same FDA submission

These recalls involve devices cleared under K043310. One submission often covers many models, so check the product and lot details in each record.

  • Z-0681-2017 · Nov 1, 2016 · Terminated
    Synthes 0.76 mm Drill Bit/Stryker J-Latch/with 5mm Stop/44.5 mm Non-Sterile
  • Z-2783-2016 · Jun 24, 2016 · Terminated
    Light Adaptor for Small Battery Drive and Small Battery Drive II.
  • Z-2784-2016 · Jun 24, 2016 · Terminated
    Adaptor for Small Battery Drive and Small Battery Drive II. Product Usage: The Light Adaptor for Small Battery Drive (SBD) /Small Battery Drive II (SBD II) is designed for use in
  • Z-2199-2016 · May 31, 2016 · Terminated
    Part # 313.250, 1.1mm Drill Bit, Mini QC with 4mm Stop/44.5mm, lot # 4326989, mfg. 9/28/2001 Product Usage: The DePuy Synthes MR Safe Instruments and MR conditional Instruments ar
  • Z-1313-2015 · Dec 19, 2014 · Terminated
    Synthes Electric Pen Drive (EPD) System, The Synthes Electric Pen Drive is indicated for screw insertion, pin and wire replacement, cutting of bone and metal, drilling, decorticati
  • Z-0615-2014 · Apr 15, 2013 · Terminated
    Synthes Hand Switch - Electric Pen Drive, Part Number 05.001.012 The Synthes Electric Pen Drive is indicated for screw insertion, pin and wire replacement, cutting of bone and met

Other DRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE, POWERED) devices

All DRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE, POWERED) devices →

Sources and updates

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