Get the free urgent medical device recall - Zimmer Biomet
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December 6, 2022, To:Risk Managers and SurgeonsSubject:URGENT MEDICAL DEVICE RECALLZimmer Biome is conducting a voluntary medical device recall related to the Bergen Stemmed Option Tibial Components
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How to fill out urgent medical device recall
How to fill out urgent medical device recall
01
Identify the urgent medical device recall notice and review all instructions carefully.
02
Gather all relevant information such as lot numbers, serial numbers, and model numbers of the affected devices.
03
Contact the manufacturer or distributor as instructed in the recall notice.
04
Follow the instructions for returning the affected devices or taking other necessary actions.
05
Keep records of all communications and actions taken related to the urgent medical device recall.
Who needs urgent medical device recall?
01
Healthcare facilities that have purchased or are using the affected medical devices.
02
Patients who have been implanted with or are using the affected medical devices.
03
Medical professionals who have prescribed or recommended the affected devices for their patients.
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What is urgent medical device recall?
Urgent medical device recall is a process of removing or correcting a medical device that is in violation of laws or regulations to avoid serious health consequences.
Who is required to file urgent medical device recall?
Manufacturers, distributors, importers, and device user facilities are required to file urgent medical device recalls.
How to fill out urgent medical device recall?
To fill out urgent medical device recall, the responsible party must provide information about the device, the reason for recall, the potential health consequences, and the actions to be taken.
What is the purpose of urgent medical device recall?
The purpose of urgent medical device recall is to protect public health and safety by removing or correcting devices that pose a risk.
What information must be reported on urgent medical device recall?
Information such as device identification, reason for recall, health consequences, and corrective actions must be reported on urgent medical device recall.
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