MAUDE Adverse Event Report: STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP MICRODRILL STRAIGHT ATTACHMENT; UNIT, OPERATIVE DENTAL

Catalog Number	5100015250
Medical Device Problem Code	Fracture (1260)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
This record is a consolidation of records summarized as a part of the fda voluntary malfunction summary reporting program.Reported events 9 events were reported for this quarter.Product return status 7 devices were received.2 devices had investigation types that have not yet been determined.Evaluation findings (results/components) 4 devices: fracture problem / bearings 1 device: wear problem / bearings 2 devices: results pending completion of investigation / part/component/sub-assembly term not applicable 1 device: fracture problem / part/component/sub-assembly term not applicable 1 device: wear problem / part/component/sub-assembly term not applicable product disposition 7 devices: scrapped by stryker 2 devices: product disposition is not yet determined additional information 9 devices were not labeled for single-use.9 devices were not reprocessed or reused.
Event or Problem Description
This record is a consolidation of records summarized as a part of the fda voluntary malfunction summary reporting program.Events occurred between july 1 ¿ september 30 2025.This report summarizes 9 events for the failure: fracture.- 8 events had problem identified during non-clinical procedure; there was no patient involvement.- 1 event had no health consequences or impact.
Additional Manufacturer Narrative
This record is a consolidation of records summarized as a part of the fda voluntary malfunction summary reporting program.Mfr report # 3015967359-2025-99459.Supplemental rationale: corrected data: b5, h1, h6, h11.9 events were previously reported during the reporting quarter; however, 2 events were reported in error.7 previously reported events are included in this follow-up record.Product return status: 7 devices were received.Evaluation findings (results/components): 4 devices: fracture problem / bearings.1 device: wear problem / bearings.1 device: fracture problem / part/component/sub-assembly term not applicable.1 device: wear problem / part/component/sub-assembly term not applicable.Product disposition 7 devices: scrapped by stryker.
Event or Problem Description
This record is a consolidation of records summarized as a part of the fda voluntary malfunction summary reporting program.Events occurred between july 1 ¿ september 30 2025.This report summarizes 7 events for the failure: fracture.7 events had problem identified during non-clinical procedure; there was no patient involvement.

• Brand Name: MICRODRILL STRAIGHT ATTACHMENT
• Common Device Name: UNIT, OPERATIVE DENTAL
• Manufacturer (Section D): STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP; 1941 stryker way; portage MI 49002
• Manufacturer (Section G): STRYKER INSTRUMENTS-KALAMAZOO; 4100 east milham avenue; kalamazoo MI 49001
• Manufacturer Contact: kelsey barla ; 1941 stryker way; portage, MI 49002 ; 2693237700
• MDR Report Key: 23399767
• Report Number: 3015967359-2025-99459
• Device Sequence Number: 9983594
• Product Code: EIA
• UDI-Device Identifier: 04546540380272
• UDI-Public: 04546540380272
• Combination Product (Y/N): N
• Initial Reporter State: MI
• Initial Reporter Country: US
• Exemption Number: VMSR
• Number of Events Summarized: 7
• Summary Report (Y/N): Y
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 01/27/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Catalogue Number: 5100015250
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 09/30/2025
• Supplement Date Received by Manufacturer: 09/30/2025
• Initial Report FDA Received Date: 10/28/2025
• Supplement Report FDA Received Date: 01/27/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Is the Device Labeled for Single Use? (Y/N): No
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Patient Sex: Unknown