MAUDE Adverse Event Report: STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP ELITE 7CM ANGLED ATTACHMENT; DRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE, POWERED)

Catalog Number	5407120452
Medical Device Problem Code	Detachment of Device or Device Component (2907)
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: 4 events were reported for this quarter.Product return status: 1 device was not available for evaluation.1 device investigation type has not yet been determined.2 devices were received.Evaluation findings (results/components): 1 device: no findings available / part/component/sub-assembly term not applicable.1 device: results pending completion of investigation / part/component/sub-assembly term not applicable.2 devices: wear problem / bearings.Product disposition: 1 device: product not received.2 devices: scrapped by stryker.1 device: product disposition is not yet determined.Additional information: 4 devices were not labeled for single-use.4 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 (b)(6) 2026.This report summarizes 4 events for the failure: detachment of device or device component.- 1 event had no health consequences or impact.- 3 events had problem identified during non-clinical procedure; there was no patient involvement.
Additional Manufacturer Narrative
This record is a consolidation of records summarized as a part of the fda voluntary malfunction summary reporting program.Mfr report # 3015967359-2026-99305.Supplemental rationale: corrected data: b5, h6, h11.4 previously reported events were included in this follow-up record.Product return status: 1 device was not available for evaluation.3 devices were received.Evaluation findings (results/components): 1 device: no findings available / part/component/sub-assembly term not applicable.1 device: degradation problem identified / bearings.2 devices: wear problem / bearings.Product disposition: 1 device: product not received.3 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 january 1 ¿ march 31 2026.This report summarizes 4 events for the failure: detachment of device or device component.- 1 event had no health consequences or impact.- 3 events had problem identified during non-clinical procedure; there was no patient involvement.
Additional Manufacturer Narrative
This record is a consolidation of records summarized as a part of the fda voluntary malfunction summary reporting program.Mfr report # 3015967359-2026-99305.Supplemental rationale: corrected data: b5, h6, h11.4 previously reported events were included in this follow-up record.Product return status: 1 device was not available for evaluation.3 devices were received.Evaluation findings (results/components): 1 device: no findings available / part/component/sub-assembly term not applicable.1 device: degradation problem identified / bearings.2 devices: wear problem / bearings.Product disposition: 1 device: product not received.3 devices: scrapped by stryker.
Event or Problem Description
No change.

• Brand Name: ELITE 7CM ANGLED ATTACHMENT
• Common Device Name: DRILLS, BURRS, TREPHINES & ACCESSORIES (SIMPLE, POWERED)
• 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: 24954394
• Report Number: 3015967359-2026-99305
• Device Sequence Number: 5406678
• Product Code: HBE
• UDI-Device Identifier: 07613327096552
• UDI-Public: 07613327096552
• Combination Product (Y/N): N
• Initial Reporter State: MI
• Initial Reporter Country: US
• Exemption Number: VMSR
• Number of Events Summarized: 4
• Summary Report (Y/N): Y
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup,Followup
• Report Date (Section B): 04/28/2026

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: 5407120452
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 03/31/2026
• Supplement Date Received by Manufacturer: 03/31/2026; 03/31/2026
• Initial Report FDA Received Date: 04/22/2026
• Supplement Report FDA Received Date: 04/27/2026; 04/28/2026
• Was Device Evaluated by Manufacturer? (Y/N): No
• 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