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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MASIMO - 40 PARKER USPO2 PULSE OXIMETRY CABLE KIT; OXIMETER
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MASIMO - 40 PARKER USPO2 PULSE OXIMETRY CABLE KIT; OXIMETER Back to Search Results
Model Number 3577
Medical Device Problem Code Sensing Intermittently (1558)
Health Effect - Clinical Code No Consequences Or Impact To Patient (2199)
Date of Event 01/01/1901
Type of Reportable Event Malfunction
Additional Manufacturer Narrative
The returned cable was evaluated.Visual inspection upon receiving revealed a damaged cable cover relief.The cable failed functional testing.The cable had an intermittent connection and loses power when twisted, shaken or bent due to damage to the cable in the ch connector area.A service history record review reveals that this unit was in the field for over one (1) year with no previous reported issues related to this reported event.
 
Event or Problem Description
The customer reported an intermittent operation, when the cable is moved the signal is lost.No patient impact or consequences were reported.
 
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Brand Name
USPO2 PULSE OXIMETRY CABLE KIT
Common Device Name
OXIMETER
Manufacturer (Section D)
MASIMO - 40 PARKER
40 parker
irvine CA 92618 1604
MDR Report Key8324075
Report Number2031172-2019-00073
Device Sequence Number13834810
Product Code DQA
UDI-Device Identifier00843997007481
UDI-Public00843997007481
Combination Product (Y/N)N
Initial Reporter StateCO
Initial Reporter CountryUS
PMA/510(K) Number
K121914
Number of Events Summarized1
Summary Report (Y/N)N
Reporter Type Manufacturer
Report Source health professional,user faci
Initial Reporter Occupation Biomedical Engineer
Remedial Action Other
Type of Report Initial
Report Date (Section B) 01/17/2019
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
Operator of Device Health Professional
Device Model Number3577
Device Catalogue Number3577
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer01/25/2019
Was the Report Sent to FDA? No
Type of Report(Section G)Thirty-Day
Initial Date Received by Manufacturer 01/17/2019
Initial Report FDA Received Date02/08/2019
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)		 No
Patient Sequence Number1
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