MAUDE Adverse Event Report: STRYKER MEDICAL-KALAMAZOO PROCUITY ZMX WITH ISOLIBRIUM; BED, AC-POWERED ADJUSTABLE HOSPITAL

Catalog Number	3009PX-ZMX-600
Medical Device Problem Codes	Unintended System Motion (1430); Patient Device Interaction Problem (4001)
Health Effect - Clinical Code	Bruise/Contusion (1754)
Date of Event	04/01/2024
Type of Reportable Event	Malfunction
Event or Problem Description
This report summarizes 1 malfunction event, where it was reported the device experienced unintended direction of the zoom and user entrapped in component.There was 1 event with patient involvement; the patient experienced bruise/contusion.
Additional Manufacturer Narrative
This record is a consolidation of records summarized as part of the fda voluntary malfunction summary reporting program.1 device was functionally/visually inspected in the field.The device was repaired and returned to use.There was no remedial action taken.This device is not labeled for single use.
Additional Manufacturer Narrative
This supplemental is being filed to remove a results code following the completion of a device investigation.Section h codes have been updated.
Event or Problem Description
This report summarizes 1 malfunction event, where it was reported the device experienced unintended direction of the zoom and user entrapped in component.There was 1 event with patient involvement; the patient experienced bruise/contusion.

• Brand Name: PROCUITY ZMX WITH ISOLIBRIUM
• Common Device Name: BED, AC-POWERED ADJUSTABLE HOSPITAL
• 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: melissa simon ; 3800 east centre avenue; portage, MI 49002 ; 2693292100
• MDR Report Key: 19838469
• Report Number: 0001831750-2024-00936
• Device Sequence Number: 17834870
• Product Code: FNL
• UDI-Device Identifier: 07613327541328
• UDI-Public: 07613327541328
• Combination Product (Y/N): N
• Initial Reporter State: MI
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): Y
• Reporter Type: Manufacturer
• Report Source: Company Representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 10/22/2024

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: 3009PX-ZMX-600
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: No
• Type of Report(Section G): Initial
• Initial Date Received by Manufacturer: 07/01/2024
• Supplement Date Received by Manufacturer: 07/01/2024
• Initial Report FDA Received Date: 07/26/2024
• Supplement Report FDA Received Date: 10/22/2024
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• 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