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Dear Distributor, Philips has determined that the M3539A AC Power Module for the HeartS tart Mr Monitor/Defibrillator may fail at a higher than expected rate. These failures were due to either an
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Fill out the form with accurate and complete information
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Provide relevant details such as customer name, product details, and recall reason
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Who needs class i recall heartstart?

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Individuals or organizations who have purchased or used the Class I Recall Heartstart product
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Users who have identified potential risks or defective aspects related to the product
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Customers who have received recall notifications from the product manufacturer or authorities
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Anyone involved in the distribution, sales, or servicing of the Class I Recall Heartstart product

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A Class I recall for HeartStart refers to a serious issue with a medical device that poses a significant risk to health, requiring immediate action.
Manufacturers and distributors of the HeartStart device are required to file a Class I recall with the appropriate regulatory authorities.
To fill out a Class I recall for HeartStart, manufacturers must complete the required forms and provide detailed information about the device, the issue, and the corrective actions taken.
The purpose of a Class I recall for HeartStart is to protect public health by informing users about potential risks and ensuring that defective devices are removed from circulation.
Information that must be reported includes the product details, the nature and risks associated with the defect, steps for users to take, and measures for correcting the issue.
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