MAUDE Adverse Event Report: MASIMO - 40 PARKER LNCS INF-L; OXIMETER

Model Number	2320
Medical Device Problem Code	Device Stops Intermittently (1599)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	04/10/2017
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The returned sensor was evaluated.During evaluation the sensor passed all visual and functional testing.The sensor was determined to be functioning as designed.
Event or Problem Description
The customer reported, ¿i had another sensor that was provided to me that was working on an icu patient, then all of a sudden stopped working, and did not alarm on the ge monitor on west 4.This has been consistent with feedback from west 3 and west 4.This is our 5th sensor that this has occurred with." the account states that the nurse saw the sensor flat-line with no alarm sounding by the ge monitor.No consequences or impact to patient were reported.

• Brand Name: LNCS INF-L
• Common Device Name: OXIMETER
• Manufacturer (Section D): MASIMO - 40 PARKER; 40 parker; irvine CA 92618 1604
• MDR Report Key: 6529704
• Report Number: 2031172-2017-00520
• Device Sequence Number: 796999
• Product Code: DQA
• UDI-Device Identifier: 10843997000892
• UDI-Public: (01)10843997000892(17)200201(10)K17BJZ
• Combination Product (Y/N): N
• Initial Reporter State: WI
• Initial Reporter Country: US
• PMA/510(K) Number: K101896
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: health professional,user faci
• Initial Reporter Occupation: Other Health Care Professional
• Remedial Action: Other
• Type of Report: Initial

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: 2320
• Device Catalogue Number: 1861
• Device Lot Number: K17BJZ
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 04/19/2017
• Was the Report Sent to FDA?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 04/10/2017
• Initial Report FDA Received Date: 04/28/2017
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1