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September 25, 2019, To:Hospital and SurgeonsSubject:URGENT MEDICAL DEVICE FIELD SAFETY NOTICE REMOVAL SPECIFICAffected Product:Various Legacy Biome ProductsReference: MFA 201900136Purpose of this

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How to fill out zimmer biomet recalls rosa

01

Obtain the Zimmer Biomet Recalls ROSA notification from the manufacturer.

02

Identify the affected ROSA product model and serial numbers.

03

Review the reason for the recall and any potential risks associated with the product.

04

Complete the required forms provided by Zimmer Biomet, including providing contact information and details about the affected product.

05

Follow any instructions for returning the affected product or taking other necessary actions.

Who needs zimmer biomet recalls rosa?

01

Patients who have received a Zimmer Biomet ROSA product that is included in the recall.

02

Healthcare professionals who have implanted or used Zimmer Biomet ROSA products on patients.

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What is zimmer biomet recalls rosa?

Zimmer Biomet recalls rosa is a process initiated by Zimmer Biomet to address any safety concerns or issues related to their ROSA robotic surgical system.

Who is required to file zimmer biomet recalls rosa?

Healthcare facilities and providers who use the ROSA robotic surgical system are required to file zimmer biomet recalls rosa.

How to fill out zimmer biomet recalls rosa?

Healthcare facilities and providers can fill out zimmer biomet recalls rosa by following the instructions provided by Zimmer Biomet and submitting the required information.

What is the purpose of zimmer biomet recalls rosa?

The purpose of zimmer biomet recalls rosa is to ensure the safety and effectiveness of the ROSA robotic surgical system by addressing any potential issues or concerns.

What information must be reported on zimmer biomet recalls rosa?

The information reported on zimmer biomet recalls rosa may include details of any incidents or adverse events related to the ROSA robotic surgical system, as well as any actions taken to address these issues.

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