STATIC AND DYNAMIC COMPLIANCE 22 E 777404-101

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2016-10-24 for STATIC AND DYNAMIC COMPLIANCE 22 E 777404-101 manufactured by Carefusion, Inc.

Event Text Entries

[58525179] (b)(4). Results of investigation: the carefusion failure analysis lab received the suspected component and performed a failure investigation. Visual examination of the mass flow board, as received, revealed a burnt capacitor, c58. It was determined that the burnt capacitor could have caused the power cables error.
Patient Sequence No: 1, Text Type: N, H10


[58525180] The customer reported that while booting up the encore 22 e device, she received check cables and interface error messages. It is unknown if there was any patient involvement at the time of the issue.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2031702-2016-01175
MDR Report Key6051698
Date Received2016-10-24
Date of Report2016-10-24
Date of Event2014-07-18
Date Mfgr Received2016-10-12
Date Added to Maude2016-10-24
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
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 DRIVE
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 Received2016-10-24
Returned To Mfg2014-08-01
Model Number22 E
Catalog Number777404-101
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerCAREFUSION, INC
Manufacturer Address1100 BIRD CENTER DRIVE PALM SPRINGS CA 92262 US 92262


Patients

Patient NumberTreatmentOutcomeDate
10 2016-10-24

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