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September 22, 2021, To:Hospital Risk Managers and SurgeonsSubject:URGENT MEDICAL DEVICE CORRECTIONAffected Product:ROSA One 3.1 Brain applicationItem NumberSerial NumberROSAS002XXBSYYZZZUDI Numbers
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How to fill out zimmer biomet recall rosa
How to fill out zimmer biomet recall rosa
01
Contact Zimmer Biomet recall department for instructions on how to fill out the form.
02
Provide all requested information on the form accurately.
03
Submit the form as per the given instructions.
Who needs zimmer biomet recall rosa?
01
Patients who have received Zimmer Biomet rosa implants and need to be part of the recall process.
02
Medical professionals who are involved in the care of patients with Zimmer Biomet rosa implants.
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What is zimmer biomet recall rosa?
Zimmer Biomet Recall Rosa refers to a recall initiated by Zimmer Biomet regarding a specific product or medical device named Rosa.
Who is required to file zimmer biomet recall rosa?
Medical facilities, healthcare providers, and distributors who have purchased or used the affected Rosa product are required to file the Zimmer Biomet Recall Rosa.
How to fill out zimmer biomet recall rosa?
To fill out the Zimmer Biomet Recall Rosa, individuals must provide detailed information about the affected product, the reason for the recall, any adverse events associated with the product, and contact information for the person filing the report.
What is the purpose of zimmer biomet recall rosa?
The purpose of the Zimmer Biomet Recall Rosa is to ensure patient safety by identifying and addressing any issues or defects with the affected medical device.
What information must be reported on zimmer biomet recall rosa?
Information such as the product name, lot number, reason for the recall, any adverse events reported, and contact information for the person filing the report must be included in the Zimmer Biomet Recall Rosa.
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