FDA Adverse Event Malfunction Summary report: N

WAVE CLINICAL PLATFORM

MDR report key: 17379329 · Received July 24, 2023

Report

Report Number
2027454-2023-00060
Event Type
Malfunction
Date Received
July 24, 2023
Date of Event
June 26, 2023
Report Date
October 3, 2023
Manufacturer
HILL-ROM CARY
Product Code
MWI
UDI-DI
00856128007007
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
TN, US
Reporter Occupation
OTHER
Health Professional
N

Narratives

Additional Manufacturer Narrative · 0

THE WAVE CLINICAL PLATFORM IS SOFTWARE INTENDED TO ROUTE, STORE, AND DISPLAY DATA, ALARMS, RESULTS AND DIAGNOSTIC INFORMATION FROM MEDICAL DEVICES, ELECTRONIC MEDICAL RECORDS (EMR), AND CLINICAL INFORMATION SYSTEMS (CIS). THE WAVE CLINICAL PLATFORM IS A REMOTE MONITORING PLATFORM THAT DISPLAYS PHYSIOLOGIC DATA, WAVEFORMS, ALARMS, RESULTS AND DIAGNOSTIC INFORMATION ROUTED THROUGH THE PLATFORM FROM SUPPORTED DEVICES AND SYSTEMS. THE WAVE CLINICAL PLATFORM IS INTENDED FOR USE IN HOSPITAL OR HOSPITAL TYPE ENVIRONMENTS. THE WAVE CLINICAL PLATFORM IS INTENDED TO BE USED BY HEALTHCARE PROFESSIONALS FOR THE FOLLOWING PURPOSES: ¿ TO REMOTELY CONSULT REGARDING PATIENTS¿ STATUSES; ¿ TO REMOTELY REVIEW OTHER STANDARD OR CRITICAL NEAR REAL-TIME PATIENT DATA, WAVEFORMS, ALARMS, AND RESULTS IN ORDER TO UTILIZE THIS INFORMATION TO AID IN CLINICAL DECISIONS. THE USER MANUAL CONTAINS WARNINGS SUCH AS "THE WAVE CLINICAL PLATFORM IS INTENDED TO SUPPLEMENT AND NOT REPLACE ANY PART OF THE HOSPITAL'S DEVICE MONITORING OR ELECTRONIC DATA MANAGEMENT SYSTEMS. DO NOT RELY ON THE WAVE CLINICAL PLATFORM PRODUCT AS THE SOLE SOURCE OF ALARMS" THE HRC TECHNICIAN UPGRADED THE WAVE FOR THE CUSTOMER TO RESOLVE THE ISSUE. ALTHOUGH THERE WAS NO INJURY ASSOCIATED WITH THIS EVENT, IF THE REPORTED ISSUE WERE TO RECUR IT COULD LEAD TO INJURY OR DEATH. THEREFORE HILLROM IS REPORTING THIS COMPLAINT.

Additional Manufacturer Narrative · 0

THE WAVE CLINICAL PLATFORM IS SOFTWARE INTENDED TO ROUTE, STORE, AND DISPLAY DATA, ALARMS, RESULTS AND DIAGNOSTIC INFORMATION FROM MEDICAL DEVICES, ELECTRONIC MEDICAL RECORDS (EMR), AND CLINICAL INFORMATION SYSTEMS (CIS). THE WAVE CLINICAL PLATFORM IS A REMOTE MONITORING PLATFORM THAT DISPLAYS PHYSIOLOGIC DATA, WAVEFORMS, ALARMS, RESULTS, AND DIAGNOSTIC INFORMATION ROUTED THROUGH THE PLATFORM FROM SUPPORTED DEVICES AND SYSTEMS. THE WAVE CLINICAL PLATFORM IS INTENDED FOR USE IN HOSPITAL OR HOSPITAL TYPE ENVIRONMENTS. THE WAVE CLINICAL PLATFORM IS INTENDED TO BE USED BY HEALTHCARE PROFESSIONALS FOR THE FOLLOWING PURPOSES: ¿ TO REMOTELY CONSULT REGARDING PATIENTS¿ STATUSES. ¿ TO REMOTELY REVIEW OTHER STANDARD OR CRITICAL NEAR REAL-TIME PATIENT DATA, WAVEFORMS, ALARMS, AND RESULTS IN ORDER TO UTILIZE THIS INFORMATION TO AID IN CLINICAL DECISIONS. THE WAVE CLINICAL PLATFORM IS INTENDED TO SUPPLEMENT AND NOT REPLACE ANY PART OF THE HOSPITAL'S DEVICE MONITORING OR ELECTRONIC DATA MANAGEMENT SYSTEMS. DO NOT RELY ON THE WAVE CLINICAL PLATFORM PRODUCT AS THE SOLE SOURCE OF ALARMS. THE INVESTIGATION IS ONGOING, HOWEVER IF ANY ADDITIONAL RELEVANT INFORMATION IS IDENTIFIED FOLLOWING COMPLETION OF THE INVESTIGATION, THE ADDITIONAL RELEVANT INFORMATION WILL BE SUBMITTED IN A SUPPLEMENTAL REPORT.

Description of Event or Problem · 0

IT WAS REPORTED THAT THE CUSTOMER RECEIVED A WEBSOCKET 1006 ERROR AND MESSAGE WAS NEVER SENT IN A DISPATCH EVENT. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).

Description of Event or Problem · 0

IT WAS REPORTED THAT THE CUSTOMER RECEIVED A WEBSOCKET 1006 ERROR AND MESSAGE WAS NEVER SENT IN A DISPATCH EVENT. THIS REPORT WAS FILED IN OUR COMPLAINT HANDLING SYSTEM AS COMPLAINT # (B)(4).

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
864811 WAVE CLINICAL PLATFORM MONITOR, PHYSIOLOGICAL, PATIENT (WITHOUT ARRHYTHMIA DETECTION OR ALARMS) MWI HILL-ROM CARY 00856128007007

Patients

Seq Age Sex Outcome Treatment
1 Unknown