MAUDE Adverse Event Report: PHILIPS NORTH AMERICA LLC FR3 DEFIBRILLATOR TEXT, EU (T), EXCHANGE; AED

Model Number 861388

Device Problem Inaudible or Unclear Audible Prompt/Feedback (2283)

Patient Problem No Clinical Signs, Symptoms or Conditions (4582)

Event Type  malfunction  

Event Description

It has been reported that the device is failing self-test.

• Brand Name: FR3 DEFIBRILLATOR TEXT, EU (T), EXCHANGE
• Type of Device: AED
• Manufacturer (Section D): PHILIPS NORTH AMERICA LLC; 22100 bothell everett highway; bothell WA 98021
• Manufacturer (Section G): PHILIPS NORTH AMERICA LLC; 22100 bothell everett highway; bothell WA 98021
• Manufacturer Contact: dana tackett ; 22100 bothell everett highway; bothell, WA 98021 ; 9095703538
• MDR Report Key: 12390478
• MDR Text Key: 268878674
• Report Number: 3030677-2021-13987
• Device Sequence Number: 1
• Product Code: MKJ
• UDI-Device Identifier: 00884838049987
• UDI-Public: 00884838049987
• Combination Product (y/n): N
• Reporter Country Code: FR
• PMA/PMN Number: P160028
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: distributor,foreign
• Reporter Occupation: Other
• Type of Report: Initial

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 08/31/2021
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Other
• Device Model Number: 861388
• Device Catalogue Number: 453564402741
• Was Device Available for Evaluation?: No
• Distributor Facility Aware Date: 08/20/2021
• Date Manufacturer Received: 08/20/2021
• Was Device Evaluated by Manufacturer?: Device Not Returned to Manufacturer
• Date Device Manufactured: 02/01/2015
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: N
• Patient Sequence Number: 1