NA 317.72Recalls & reported problems
Synthes GmbH · 1.5MM DRILL BIT/STRYKER J-LTCH WITH 12MM STOP/44.5MM · Class 2
- 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 10887587038674), received between Nov 3, 2023 and Nov 3, 2023 — classified as 1 malfunction.
The most frequently reported specific device problem is “Break” (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
- Break1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 3, 2023Break; Break
DEVICE REPORT FROM HONG KONG REPORTS AN EVENT AS FOLLOWS: IT WAS REPORTED THAT ON (B)(6) 2023 DURING AN UNKNOWN PROCEDURE, THE DRILL BIT IN QUESTION BROKE. THERE WAS NO SURGICAL DELAY, ALL FRAGMENTS GENERATED WERE REMOVED WITHOUT ADDITIONAL MEDICAL INTERVENTION. THE PROCEDURE WAS COMPLETED SUCCESSFULLY WITH NO ADVERSE PATIENT IMPACT. THIS REPORT IS FOR A 1.5MM DRILL BIT/STRYKER J-LTCH WITH 12MM STOP/44.5MM. THIS IS REPORT 1 OF 1 FOR (B)(4).
Patient problems: Insufficient Information
MAUDE report 18067908 ↗
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: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.