MAUDE Adverse Event Report: STRYKER SPINE-US NAVIGATION ENABLED SERRATO/ES2/XIA 3 DRIVER, CANNULATED; ORTHOPEDIC STEREOTAXIC INSTRUMENT

Catalog Number	48702681
Medical Device Problem Codes	Fracture (1260); Difficult to Insert (1316); Naturally Worn (2988)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	02/20/2026
Type of Reportable Event	Malfunction
Event or Problem Description
A company representative reported that a navigation enabled serrato/es2/xia 3 driver was loose when engaging with a screw intra-operatively and that the tip appeared worn.The procedure was completed successfully with no surgical delay and no adverse consequence to the patient.
Event or Problem Description
Inspection of the returned device indicates that several prongs on the device tip had fractured off.
Additional Manufacturer Narrative
Additional data: b5, h3.H6 coding has been updated to reflect completion of the investigation.

• Brand Name: NAVIGATION ENABLED SERRATO/ES2/XIA 3 DRIVER, CANNULATED
• Common Device Name: ORTHOPEDIC STEREOTAXIC INSTRUMENT
• Manufacturer (Section D): STRYKER SPINE-US; 2 pearl court; allendale NJ 07401
• Manufacturer (Section G): STRYKER SPINE-FRANCE; zone industrielle de marticot; cestas 33610 ; FR 33610
• Manufacturer Contact: catherine devarenne ; 2 pearl court; allendale, NJ 07401 ; 2017608000
• MDR Report Key: 24542057
• Report Number: 0009617544-2026-00033
• Device Sequence Number: 5688910
• Product Code: OLO
• UDI-Device Identifier: 07613327460964
• UDI-Public: (01)07613327460964(11)220923(10)221530
• Combination Product (Y/N): N
• Initial Reporter State: OH
• Initial Reporter Country: US
• PMA/510(K) Number: K183381
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Serviced by Third Party (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 04/02/2026

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 Catalogue Number: 48702681
• Device Lot Number: 221530
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 03/03/2026
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 02/20/2026
• Supplement Date Received by Manufacturer: 04/01/2026
• Initial Report FDA Received Date: 03/08/2026
• Supplement Report FDA Received Date: 04/03/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 09/23/2022
• 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