MAUDE Adverse Event Report: NIHON KOHDEN TOMIOKA CORPORATION AG-920RA; MULTI-GAS UNIT

Model Number AG-920RA

Device Problem Device Inoperable (1663)

Patient Problem No Known Impact Or Consequence To Patient (2692)

Event Date 09/18/2015

Event Type  malfunction  

Manufacturer Narrative

The customer went through the process of calibrating the multi-gas unit per the manual and the readings are not coming back as accurate.The device was returned to nihon (b)(4), evaluated, and the reported issue was not able to be confirmed or duplicated.The device passed all gas specifications and calibrations.The device will be returned to the customer.Nihon (b)(4) will submit a supplemental report in accordance with 21 cfr section 803.56 if additional information becomes available.

Event Description

The customer went through the process of calibrating the multi-gas unit per the manual and the readings are not coming back as accurate.

• Brand Name: AG-920RA
• Type of Device: MULTI-GAS UNIT
• Manufacturer (Section D): NIHON KOHDEN TOMIOKA CORPORATION; 486 nanokaichi; tomioka city, japan 370-2 343; JA 370-2343
• Manufacturer (Section G): NIHON KOHDEN TOMIOKA CORPORATION; 486 nanokaichi; tomioka city, japan 370-2 343; JA 370-2343
• Manufacturer Contact: thomas bento ; 1-31-4 nishiochia, shinjuku-ku; tokyo, japan 161-8-560 ; JA 161-8560 ; 2687708
• MDR Report Key: 5158601
• MDR Text Key: 28557698
• Report Number: 8030229-2015-00311
• Device Sequence Number: 1
• Product Code: CCK
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K023475
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: user facility
• Reporter Occupation: Biomedical Engineer
• Report Date: 10/18/2015,09/18/2015

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
• Device Operator: Health Professional
• Device Model Number: AG-920RA
• Device Catalogue Number: AG-920RA
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 10/05/2015
• Is the Reporter a Health Professional?: Yes
• Was the Report Sent to FDA?: Yes
• Date Report Sent to FDA: 10/18/2015
• Distributor Facility Aware Date: 09/18/2015
• Device Age: 43 MO
• Event Location: Hospital
• Date Report to Manufacturer: 10/18/2015
• Initial Date Manufacturer Received: Not provided
• Initial Date FDA Received: 10/18/2015
• Was Device Evaluated by Manufacturer?: Yes
• Date Device Manufactured: 02/13/2012
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Reuse
• Patient Sequence Number: 1