NA S-5D-G1Recalls & reported problems
Synthes GmbH · 5 mm Diamond Ball. Use with QD8-G1, SHORT-G1, QD8, QD8-S, SHORT Attachments. · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00845384012696), received between Jan 19, 2022 and Jul 6, 2023 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Separation Problem” (2 reports).
39 other recalls cover devices cleared under the same FDA submission (K113476); 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
- Separation Problem2
- Device Damaged by Another Device1
- Material Deformation1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 6, 2023Device Damaged by Another Device; Separation Problem; Device Damaged by Another Device; Separation Problem
IT WAS REPORTED FROM SWITZERLAND THAT DURING SERVICE AND EVALUATION, IT WAS DETERMINED THAT THE CUTTER DEVICE FAILED VISUAL INSPECTION DUE TO A WORN CUTTING EDGE (CUTTER DAMAGED). IT WAS FURTHER DETERMINED THAT THE DEVICE FAILED PRETEST FOR CHECK FOR SAFETY, CHECK FOR UNTRUE RUNNING AND CHECK FOR GENERAL CONDITION. IT WAS NOTED IN THE SERVICE ORDER THAT THE CUTTER DEVICE COULD NOT DISENGAGE FROM THE ATTACHMENT AND MOTOR DEVICE. THIS EVENT DID NOT OCCUR DURING SURGERY. THERE WAS NO PATIENT INVOLVEMENT. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, A SUPPLEMENTAL MEDWATCH WILL BE SUBMITTED ACCORDINGLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 17271826 ↗MalfunctionJan 19, 2022Material Deformation; Separation Problem; Material Deformation; Separation Problem
IT WAS REPORTED FROM (B)(6) THAT DURING SERVICE AND EVALUATION, IT WAS DETERMINED THAT THE CUTTER DEVICE COATING WAS PARTIALLY DAMAGED AND TRACES OF RESIDUE COULD BE FOUND ON THE SHAFT. IT WAS NOTED IN THE SERVICE ORDER THAT THE DEVICE HAD BEARING DAMAGE AND THE BURR COULD NOT BE DETACHED. IT WAS ALSO REPORTED THAT THE DEVICE WAS BEING USED WITH AN ATTACHMENT DEVICE. THIS EVENT DID NOT OCCUR DURING SURGERY. THERE WAS NO PATIENT INVOLVEMENT. THERE WERE NO REPORTS OF INJURIES, MEDICAL INTERVENTION OR PROLONGED HOSPITALIZATION. ALL AVAILABLE INFORMATION HAS BEEN DISCLOSED. IF ADDITIONAL INFORMATION SHOULD BECOME AVAILABLE, AN ADDITIONAL REPORT WILL BE SUBMITTED ACCORDINGLY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 13289783 ↗
Recalls under the same FDA submission
These recalls involve devices cleared under K113476. One submission often covers many models, so check the product and lot details in each record.
- Z-2837-2016 · Aug 26, 2016 · TerminatedG1 Dissection Tool - 7mm FBALL L; For cutting and shaping bone including spine and cranium.
- Z-2839-2016 · Aug 26, 2016 · TerminatedG1 Dissection Tool - 3mm FLUTED BALL; For cutting and shaping bone including spine and cranium.
- Z-2840-2016 · Aug 26, 2016 · TerminatedG1 Dissection Tool - 6MM CRS DBALL, 2mm Shaft EXP, M; For cutting and shaping bone including spine and cranium.
- Z-2838-2016 · Aug 26, 2016 · TerminatedG1 Dissection Tool - 3mm CRS DBALL, 2mm SHAFT EXP, M; For cutting and shaping bone including spine and cranium.
- Z-2291-2015 · Apr 13, 2015 · TerminatedANSPACH - Fluted Drum, Side Cut Only; 9MM x 14 MM REF L-9DRC-G1 Cutting shaping bone including spine and cranium.
- Z-2286-2015 · Apr 13, 2015 · TerminatedANSPACH - Fluted Barrel; 8MM x 12.5MM REF L-8BA-G1 Cutting shaping bone including spine and cranium.
- Z-2301-2015 · Apr 13, 2015 · TerminatedANSPACH - 8MM x 12.5MM Fluted Barrel; REF M-8BA-G1 Cutting shaping bone including spine and cranium.
- Z-2303-2015 · Apr 13, 2015 · TerminatedANSPACH - 5MM Fluted Ball, Extends 27MM; REF M-5B-27-G1. Cutting shaping bone including spine and cranium.
- Z-2284-2015 · Apr 13, 2015 · TerminatedANSPACH - Fluted Acorn, 7MM REF L-7AC-G1 Cutting shaping bone including spine and cranium.
- Z-2293-2015 · Apr 13, 2015 · TerminatedANSPACH - 3MM Fluted Ball, 2 MM Shaft Exposure; REF M-3SB-2-G1. Cutting shaping bone including spine and cranium.
- Z-2283-2015 · Apr 13, 2015 · TerminatedANSPACH - Fluted Drum, Side Cut only, 6MM x 14MM REF L-6DRC-G1 Cutting shaping bone including spine and cranium.
- Z-2292-2015 · Apr 13, 2015 · TerminatedANSPACH - 3MM Course Diamond Ball, 2 MM Shaft Exposure; REF M-3DC-2-G1 Cutting shaping bone including spine and cranium.
- Z-2296-2015 · Apr 13, 2015 · TerminatedANSPACH - 5MM x 11.3MM Fluted Barrel; REF M-5BA-A-G1 Cutting shaping bone including spine and cranium.
- Z-2289-2015 · Apr 13, 2015 · TerminatedANSPACH - Extra Coarse Diamond Ball; 8MM REF L-8DX-G1 Cutting shaping bone including spine and cranium.
- Z-2294-2015 · Apr 13, 2015 · TerminatedANSPACH - 4MM x 11 MM Fluted Barrel, 14 Flutes; REF M-4BA-A-G1. Cutting shaping bone including spine and cranium.
…and 24 more.
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- NA 5407-FA2-000Stryker Corporation · DRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE, POWERED)181 reports
- Indigo™ 1845000Medtronic Xomed, Inc. · DRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE, POWERED)165 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 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 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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