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URGENT MEDICAL DEVICE RECALL November 07, 2019Product Field Action #:2147264Description: Crossfire 10 Degree Acetabular InsertAffected Catalog Number: 2041C3254Affected Lot Number:53778501Dear Customer,
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Visit the Medtronic website or contact the company directly to obtain the recall form for the Dual device.
02
Fill out the recall form with accurate information about the device, including serial number and reason for the recall.
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Include any additional documentation requested by Medtronic, such as medical records or proof of purchase.
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Submit the completed form and any accompanying documents to Medtronic via the specified method, such as mail or online submission.

Who needs medtronic inc recalls dual?

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Patients who have received a Medtronic inc recalls dual device and have been notified of the recall by the company.
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Medical professionals who have prescribed or implanted the Medtronic inc recalls dual device in patients.
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Medtronic Inc recalls dual refers to the company's process of recalling a medical device that has the potential to cause harm to patients.
Medtronic Inc is required to file a recall for the dual medical devices if they identify a defect or safety concern with the product.
To fill out a medtronic inc recalls dual form, the company must provide information about the affected product, the reason for the recall, potential risks to patients, and the proposed solution.
The purpose of medtronic inc recalls dual is to ensure the safety and well-being of patients who may be affected by a faulty medical device.
Information that must be reported on medtronic inc recalls dual includes the product name, lot number, reason for recall, potential risks, number of units affected, and steps taken to address the issue.
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