Matrix 03.511.310Recalls & reported problems
Synthes GmbH · MATRIX 1.4MM DRILL BIT J-LATCH/80MM · Class 2
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10887587014364), received between Jan 29, 2026 and Jan 29, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Device-Device Incompatibility” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Device-Device Incompatibility1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 29, 2026Device-Device Incompatibility
IT WAS REPORTED DURING AN ORTHOGNATHIC PROCEDURE, AFTER DRILLING WITH DRILL, THE SCREW OVER INSERTED INTO THE PLATE AND PASSED THROUGH THE PLATE. THE SURGEON WANTED TO TRY A NEW PLATE AND RE USED THE SCREW AND IT HAPPENED AGAIN. USED DIFFERENT PLATES AND SCREWS AND IT WORKED AS EXPECTED. NO PATIENT HARM AND NO SURGICAL DELAY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24210661 ↗
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 · TerminatedSynthes 0.76 mm Drill Bit/Stryker J-Latch/with 5mm Stop/44.5 mm Non-Sterile
- Z-2783-2016 · Jun 24, 2016 · TerminatedLight Adaptor for Small Battery Drive and Small Battery Drive II.
- Z-2784-2016 · Jun 24, 2016 · TerminatedAdaptor 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 · TerminatedPart # 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 · TerminatedSynthes 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 · TerminatedSynthes 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 DRILL, BONE, POWERED devices
- NA 03.505.004Synthes GmbH · DRILL, BONE, POWERED69 reports
- Nobel Biocare® 37470Nobel Biocare AB · DRILL, BONE, POWERED1 recall0 reports
- MatrixMANDIBLE 03.503.476Synthes GmbH · DRILL, BONE, POWERED26 reports
- NA 310.510Synthes GmbH · DRILL, BONE, POWERED17 reports
- NA 317.82Synthes GmbH · DRILL, BONE, POWERED16 reports
- MatrixMANDIBLE 03.503.479Synthes GmbH · DRILL, BONE, POWERED11 reports
- NA 05.001.120Synthes GmbH · DRILL, BONE, POWERED9 reports
- NA 310.520Synthes GmbH · DRILL, BONE, POWERED9 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 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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