MAUDE Adverse Event Report: MASIMO - 40 PARKER RD SET GE - 12; OXIMETER

Model Number	4085-9
Medical Device Problem Code	Incorrect Measurement (1383)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	03/31/2017
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
Attempts have been made to obtain the product.The product has not been returned to masimo to allow an analysis to be performed.If the product is returned for evaluation or new information is obtained, a follow up report will be submitted.
Event or Problem Description
It was reported that there were broken rd ge cables and questionable spo2 values.Returning 6 rd ge 4085 cables.Exposed wires at the sensor connection.No consequences or impact to patient.
Additional Manufacturer Narrative
The returned cable was evaluated.During evaluation the cable passed all visual and functional testing.The cable was determined to be functioning as designed.A service history record review reveals that this unit was in the field for over eleven (11) months with no previous reported issues related to this reported event.Corrected data: model # from "4085" to "4085-9".

• Brand Name: RD SET GE - 12
• Common Device Name: OXIMETER
• Manufacturer (Section D): MASIMO - 40 PARKER; 40 parker; irvine CA 92618 1604
• MDR Report Key: 6514090
• Report Number: 2031172-2017-00502
• Device Sequence Number: 18986433
• Product Code: DQA
• UDI-Device Identifier: 00843997009805
• UDI-Public: (01)00843997009805(11)160901(10)16JVG
• Combination Product (Y/N): N
• Initial Reporter State: MA
• Initial Reporter Country: US
• PMA/510(K) Number: K050252
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional,user faci
• Initial Reporter Occupation: Health Professional
• Remedial Action: Other
• Type of Report: Initial,Followup

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 Number: 4085-9
• Device Catalogue Number: 4085
• Device Lot Number: 16JVG
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 04/26/2017
• Was the Report Sent to FDA?: Yes
• Initial Date Received by Manufacturer: 03/31/2017
• Supplement Date Received by Manufacturer: 08/15/2017
• Initial Report FDA Received Date: 04/22/2017
• Supplement Report FDA Received Date: 08/21/2017
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1