MAUDE Adverse Event Report: STRYKER MEDICAL-KALAMAZOO TRURIZECLINICAL CHAIR; CHAIR, POSITIONING, ELECTRIC

Catalog Number	3333000000
Medical Device Problem Codes	Material Too Rigid or Stiff (1544); Adverse Event Without Identified Device or Use Problem (2993)
Health Effect - Clinical Codes	Pressure Sore/Ulcer (2326); No Clinical Signs, Symptoms or Conditions (4582)
Date of Event	07/28/2023
Type of Reportable Event	Malfunction
Event or Problem Description
The customer alleged that the trurize chair had caused pressure injuries.Attempts are being made to gather additional details from the user facility.
Additional Manufacturer Narrative
It was reported that the device's hard surfaces generate pressure was most likely not related to any component-level defect or malfunction.However, this could not be confirmed.In addition, a stryker qae spoke to a stryker sales account manager, who provided contact information for the wound care nurse who reported the complaint.Several attempts were made to obtain more information regarding the alleged events, including the number of injuries, extent of the injuries, treatment of the injuries, or resolution.However, the customer did not respond, and no additional information was gained.Based on the information provided, the alleged injuries could not be directly tied to any defect or malfunction with the product.
Event or Problem Description
It was reported that the device's hard surfaces generate pressure.

• Brand Name: TRURIZECLINICAL CHAIR
• Common Device Name: CHAIR, POSITIONING, ELECTRIC
• 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: alex wibert ; 3800 east centre avenue; portage, MI 49002 ; 2693292100
• MDR Report Key: 17627036
• Report Number: 0001831750-2023-00989
• Device Sequence Number: 7545349
• Product Code: INO
• UDI-Device Identifier: 07613327322569
• UDI-Public: 07613327322569
• Combination Product (Y/N): N
• Initial Reporter State: OR
• 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): 12/19/2023

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: Yes
• Device Catalogue Number: 3333000000
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 07/28/2023
• Supplement Date Received by Manufacturer: 07/28/2023
• Initial Report FDA Received Date: 08/25/2023
• Supplement Report FDA Received Date: 12/19/2023
• Was Device Evaluated by Manufacturer? (Y/N): No
• Date Device Manufactured: 05/30/2017
• 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
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Unknown