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Philips Healthcare___February 16, 2018 FSN86100186 Medical Device Recall/Notification HeartStart FRx, HeartStart Home, and Heartstart OnSite AEDs Dear HeartStart AED Owner, We are contacting you because
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How to fill out philips defibrillator recallaedusacom
How to fill out philips defibrillator recallaedusacom
01
Visit the official website of Philips defibrillator recall at edusacom
02
Enter your personal information such as name, address, and contact number
03
Provide the serial number of the defibrillator that is being recalled
04
Fill out the reason for the recall and any additional information requested
05
Submit the form and wait for further instructions from Philips regarding the recall process
Who needs philips defibrillator recallaedusacom?
01
Individuals or organizations who have purchased or are in possession of a Philips defibrillator that is being recalled
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What is philips defibrillator recallaedusacom?
Philips defibrillator recallaedusacom refers to the official platform or mechanism for reporting and managing the recall of Philips defibrillator devices in the United States, typically related to safety concerns or defects.
Who is required to file philips defibrillator recallaedusacom?
Manufacturers, distributors, and healthcare providers who are aware of any issues related to the Philips defibrillator devices are required to file the report.
How to fill out philips defibrillator recallaedusacom?
To fill out the philips defibrillator recallaedusacom, you need to provide details about the device, including the model number, serial number, nature of the issue, and any relevant safety information, using the designated online form or report.
What is the purpose of philips defibrillator recallaedusacom?
The purpose of philips defibrillator recallaedusacom is to ensure public safety by tracking defective devices, facilitating recalls, and preventing potential harm to patients and users.
What information must be reported on philips defibrillator recallaedusacom?
The report must include details such as the device type, model and serial numbers, description of the defect, and any incidents related to the device that may have affected patient safety.
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