TRUWAVE 896083L1B

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-04-26 for TRUWAVE 896083L1B manufactured by Edwards Lifesciences.

Event Text Entries

[143893969] The product is expected to be returned for analysis; however, it has not yet been received. Upon the return of the product a supplemental report will be sent with the investigation results as well as the device history record. Complaint histories for all reported events are reviewed against trending control limits on a monthly basis, and any excursions above the control limits are assessed and documented as part of this monthly review.
Patient Sequence No: 1, Text Type: N, H10


[143893970] As reported, during use with a patient, this truwave cable led to a misleading arterial pressure measurement. The values were about 309/200 mmhg and were not in line with the patient's clinical state. There was no error message displayed with these values. It was confirmed that the patient was not treated due to the wrong values. There was no patient details available. There was no allegation of patient injury. The cable was available for evaluation.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number2015691-2019-01503
MDR Report Key8557932
Date Received2019-04-26
Date of Report2019-04-05
Date of Event2019-03-18
Date Mfgr Received2019-06-26
Date Added to Maude2019-04-26
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 ContactMS. SAMANTHA EVELEIGH
Manufacturer StreetONE EDWARDS WAY
Manufacturer CityIRVINE CA 92614
Manufacturer CountryUS
Manufacturer Postal92614
Manufacturer Phone9492503939
Manufacturer G1EDWARDS LIFESCIENCES LLC
Manufacturer StreetONE EDWARDS WAY
Manufacturer CityIRVINE CA 92614
Manufacturer CountryUS
Manufacturer Postal Code92614
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameTRUWAVE
Generic NameTRANSDUCER, PRESSURE, CATHETER TIP
Product CodeDXO
Date Received2019-04-26
Returned To Mfg2019-06-26
Model Number896083L1B
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerEDWARDS LIFESCIENCES
Manufacturer AddressONE EDWARDS WAY IRVINE CA 92614 US 92614


Patients

Patient NumberTreatmentOutcomeDate
10 2019-04-26

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