MAUDE Adverse Event Report:; WARMER, THERMAL, INFUSION FLUID

Device Problem Failure to Calibrate (2440)

Patient Problem Insufficient Information (4580)

Event Type  malfunction  

Event Description

Information was received indicating that a smiths medical fluid warmer had an issue with calibrating the power control board (pcb).There were no reported adverse events.

Manufacturer Narrative

Returned device was received in good physical condition.During the evaluation of the device, the issue could not be duplicated.And no fault was found with the device.The device history record was reviewed and showed, that this device met all manufacturing specification for product released for distribution.No issues were identified, that would have impacted this event.

• Type of Device: WARMER, THERMAL, INFUSION FLUID
• MDR Report Key: 11969147
• MDR Text Key: 255355514
• Report Number: 3012307300-2021-05794
• Device Sequence Number: 1
• Product Code: LGZ
• Combination Product (y/n): N
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: user facility
• Type of Report: Initial,Followup
• Report Date: 07/13/2021

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
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 06/14/2021
• Was the Report Sent to FDA?: No
• Initial Date Manufacturer Received: 05/12/2021
• Initial Date FDA Received: 06/09/2021
• Supplement Dates Manufacturer Received: 06/15/2021
• Supplement Dates FDA Received: 07/13/2021
• Is This a Reprocessed and Reused Single-Use Device?: No
• Patient Sequence Number: 1