MAUDE Adverse Event Report: EMG TECHNOLOGY CO. LTD NEBULIZERS TO DELIVER AEROSOLS; 868.5630

Model Number IRC1740

Device Problem Improper Flow or Infusion (2954)

Patient Problem No Consequences Or Impact To Patient (2199)

Event Type  No Answer Provided  

Event Description

Per provider, unit cuts off.

• Brand Name: NEBULIZERS TO DELIVER AEROSOLS
• Type of Device: 868.5630
• Manufacturer (Section D): EMG TECHNOLOGY CO. LTD; no. 58, 35 rd taichung; industrial park, shituen chiu; taichung ; TW
• MDR Report Key: 4062505
• MDR Text Key: 4850835
• Report Number: 1531186-2014-03874
• Device Sequence Number: 1
• Product Code: CAF
• Combination Product (y/n): N
• Reporter Country Code: US
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: Invalid Data
• Reporter Occupation: Medical Equipment Company Technician/Representative
• Type of Report: Initial
• Report Date: 09/04/2014,08/08/2014

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: Lay User/Patient
• Device Model Number: IRC1740
• Was Device Available for Evaluation?: No
• Is the Reporter a Health Professional?: No
• Was the Report Sent to FDA?: Yes
• Date Report Sent to FDA: 09/04/2014
• Distributor Facility Aware Date: 08/08/2014
• Date Report to Manufacturer: 09/04/2014
• Initial Date Manufacturer Received: Not provided
• Initial Date FDA Received: 09/05/2014
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1
• Patient Outcome(s): Other