MAUDE Adverse Event Report: MASIMO - 40 PARKER RC-4 CABLE; OXIMETER

Model Number	2406
Medical Device Problem Code	Device Stops Intermittently (1599)
Health Effect - Clinical Code	No Consequences Or Impact To Patient (2199)
Date of Event	08/04/2017
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
The returned cable was evaluated.The returned unit passed visual inspection and continuity tests, but failed the check eeprom contents verification.During functional analysis the cable was able to generate a "replace cable" error message.(b)(6).
Event or Problem Description
The customer reported a cable intermittently would display values and then suddenly display no values with no error message.No patient impact or consequences were reported.
Additional Manufacturer Narrative
The returned cable was evaluated.The returned unit passed visual inspection and continuity tests, but failed the check eeprom contents verification.During functional analysis the cable was able to generate a "replace cable" error message.(b)(6).

• Brand Name: RC-4 CABLE
• Common Device Name: OXIMETER
• Manufacturer (Section D): MASIMO - 40 PARKER; 40 parker; irvine CA 92618 1604
• MDR Report Key: 6829467
• Report Number: 2031172-2017-00844
• Device Sequence Number: 16544371
• Product Code: DQA
• UDI-Device Identifier: 00843997000215
• UDI-Public: 00843997000215
• Combination Product (Y/N): N
• Initial Reporter Country: CA
• PMA/510(K) Number: K080238
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: foreign,health professional,u
• Initial Reporter Occupation: Biomedical Engineer
• 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: 2406
• Device Catalogue Number: 2406
• Device Lot Number: 16F44
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 08/10/2017
• Was the Report Sent to FDA?: Yes
• Initial Date Received by Manufacturer: 08/04/2017
• Supplement Date Received by Manufacturer: 08/29/2017
• Initial Report FDA Received Date: 08/30/2017
• Supplement Report FDA Received Date: 09/24/2017
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1