MAUDE Adverse Event Report: MEDTRONIC (CHANGZHOU) MEDICAL DEVICES TE SOLERA VOYAGER 5.5; SCREWDRIVER

Model Number	6550003
Medical Device Problem Code	Break (1069)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Medtronic submits this report to comply with fda regulations 21 cfr parts 4 and 803.Medtronic has made reasonable efforts to provide as much relevant information as is available to the company as of the submission date of this report.This report does not constitute an admission or a conclusion by fda, medtronic, or its employees that the device, medtronic, or its employee caused or contributed to the event described in the report.Any required fields that are unpopulated are blank because the information is currently unknown or unavailable.Medtronic will submit a supplemental report if additional relevant information becomes known.
Event or Problem Description
Information was received from user facility via a manufacturer representative regarding devices used for spinal therapy.It was repo rted that the instruments were broken and expired.There was no patient involvement reported.There were no further complications reported regarding the event.

• Brand Name: SOLERA VOYAGER 5.5
• Common Device Name: SCREWDRIVER
• Manufacturer (Section D): MEDTRONIC (CHANGZHOU) MEDICAL DEVICES TE; building #3, 11 changjiang nor; changzhou jiangsu,cn
• Manufacturer (Section G): MEDTRONIC (CHANGZHOU) MEDICAL DEVICES TE; building #3, 11 changjiang nor; changzhou jiangsu,cn
• Manufacturer Contact: justin ellis ; 1800 pyramid place; memphis, TN 38132 ; 7635265677
• MDR Report Key: 25104671
• Report Number: 3005677016-2026-00006
• Device Sequence Number: 10749866
• Product Code: HXX
• UDI-Device Identifier: 00643169754508
• UDI-Public: (01)00643169754508(11)230401(10)K22M3042
• Combination Product (Y/N): N
• Initial Reporter State: TN
• Initial Reporter Country: US
• PMA/510(K) Number: EXEMPT
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Non-Healthcare Professional
• Type of Report: Initial
• Report Date (Section B): 05/07/2026

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
• Operator of Device: Health Professional
• Device Model Number: 6550003
• Device Catalogue Number: 6550003
• Device Lot Number: K22M3042
• Was Device Available for Evaluation?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 04/09/2026
• Initial Report FDA Received Date: 05/06/2026
• Date Device Manufactured: 04/01/2023
• 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