MAUDE Adverse Event Report: Stryker Instruments-a division of Stryker Corp TPX SAGITTAL SAW; Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece

Catalog Number	7400-034-000
Medical Device Problem Code	Overheating of Device (1437)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	05/13/2026
Type of Reportable Event	Malfunction
Event or Problem Description
The manufacturer service technician reported that the device overheated while it was being serviced at the manufacturer facility.There were no adverse consequences related to this event.

• Brand Name: TPX SAGITTAL SAW
• Common Device Name: Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece
• 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: allison juday ; 1941 stryker way; portage, MI 49002 ; +1(269)323-7700
• MDR Report Key: 25256902
• Report Number: 3015967359-2026-00380
• Device Sequence Number: 21468974
• Product Code: ERL
• UDI-Device Identifier: 07613327482980
• UDI-Public: (01)07613327482980
• Combination Product (Y/N): N
• Initial Reporter State: MI
• Initial Reporter Country: US
• PMA/510(K) Number: K112593
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Type of Report: Initial,Followup
• Report Date (Section B): 08/31/2026

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: Other
• Device Catalogue Number: 7400-034-000
• Was Device Available for Evaluation?: Yes
• Date Returned to Manufacturer: 06/01/2026
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: No
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 05/13/2026
• Supplement Date Received by Manufacturer: 08/20/2026
• Initial Report FDA Received Date: 05/22/2026
• Supplement Report FDA Received Date: 08/31/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 10/01/2024
• 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