STATIC AND DYNAMIC COMPLIANCE VMAX ENCORE 229CE 24-777500

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-01-25 for STATIC AND DYNAMIC COMPLIANCE VMAX ENCORE 229CE 24-777500 manufactured by Carefusion, Inc.

Event Text Entries

[65944969] (b)(4). The customer? S biomedical engineer (biomed) examined the unit and was able to confirm the reported issue. The biomed repaired the treadmill by tightening the loose power cord connection. The customer confirmed the issue was resolved after biomed repaired the unit. Due to the event being resolved by biomed tightening the loose power cord without replacing any parts; no parts will be sent back to carefusion.
Patient Sequence No: 1, Text Type: N, H10


[65944970] The customer reported while using the vmax encore device, the treadmill would power down without warning. The issue occurred during patient use; the customer reported no patient injury associated with this event.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2021710-2017-05292
MDR Report Key6277747
Date Received2017-01-25
Date of Report2017-01-25
Date of Event2016-12-28
Date Mfgr Received2016-12-28
Device Manufacturer Date2007-09-01
Date Added to Maude2017-01-25
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactJILL RITTORNO
Manufacturer Street22745 SAVI RANCH PARKWAY
Manufacturer CityYORBA LINDA CA 92887
Manufacturer CountryUS
Manufacturer Postal92887
Manufacturer G1CAREFUSION, INC
Manufacturer Street1100 BIRD CENTER DR.
Manufacturer CityPALM SPRINGS CA 92262
Manufacturer CountryUS
Manufacturer Postal Code92262
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameSTATIC AND DYNAMIC COMPLIANCE
Generic NameCALCULATOR, PREDICTED VALUES, PULMONARY FUNCTION
Product CodeBTY
Date Received2017-01-25
Model NumberVMAX ENCORE 229CE
Catalog Number24-777500
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerCAREFUSION, INC
Manufacturer Address22745 SAVI RANCH PARKWAY YORBA LINDA CA 92887 US 92887


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2017-01-25

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.