MAUDE Adverse Event Report: STRYKER MEDICAL-KALAMAZOO PRIME ELECTRIC BIG WHEEL STRETCHER; STRETCHER, WHEELED

Catalog Number	1115000000E
Medical Device Problem Code	Mechanical Problem (1384)
Health Effect - Clinical Code	No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	04/29/2025
Type of Reportable Event	Malfunction
Event or Problem Description
It was reported that the brake pedal will not stay locked.No patient was affected and no adverse consequence or clinically relevant delay in treatment was reported.
Additional Manufacturer Narrative
Upon completion of the device evaluation by the field service technician it was identified that the initial report of the brake pedal not staying locked was reported in error and this device was not exhibiting a reportable malfunction.The device information has been updated in section d.
Event or Problem Description
It was originally reported that the brake pedal will not stay locked.Upon completion of the device evaluation by the field service technician it was identified that the initial report of the brake pedal not staying locked was reported in error and this device was not exhibiting this issue.

• Brand Name: PRIME ELECTRIC BIG WHEEL STRETCHER
• Common Device Name: STRETCHER, WHEELED
• Manufacturer (Section D): STRYKER MEDICAL-KALAMAZOO; 3800 east centre avenue; portage MI 49002
• Manufacturer (Section G): STRYKER MEDICAL-KALAMAZOO; 3800 east centre avenue; portage MI 49002
• Manufacturer Contact: brian thompson ; 3800 east centre avenue; portage, MI 49002 ; 2693292100
• MDR Report Key: 22091239
• Report Number: 0001831750-2025-00704
• Device Sequence Number: 7885096
• Product Code: FPO
• UDI-Device Identifier: 07613327278217
• UDI-Public: (01)07613327278217
• Combination Product (Y/N): N
• Initial Reporter State: OH
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: User Facility
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 07/22/2025

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: 1115000000E
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Follow-Up
• Initial Date Received by Manufacturer: 04/29/2025
• Supplement Date Received by Manufacturer: 04/29/2025
• Initial Report FDA Received Date: 05/27/2025
• Supplement Report FDA Received Date: 07/22/2025
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 06/20/2016
• 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