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18 December 2013Field Safety Notice
Urgent Medical Device Recall 295584211152013014R
Specific Lots of Large Needle Driver and Mega Needle Driver Endowment Instruments for da Vinci
Surgical SystemsIntroduction
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How to fill out recall of device recall
How to fill out recall of device recall
01
Obtain the device recall form from the manufacturer or regulatory agency.
02
Fill out the form with all the required information, such as device details, reason for the recall, affected batch numbers, and contact information.
03
Provide any supporting documentation or evidence related to the recall.
04
Submit the completed form to the manufacturer or regulatory agency as specified in the instructions.
Who needs recall of device recall?
01
Manufacturers of medical devices who are conducting a recall.
02
Healthcare facilities or providers who have received the recalled device and need to report back to the manufacturer or regulatory agency.
03
Patients or consumers who have purchased or used the recalled device and need to provide feedback or return the device.
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What is recall of device recall?
Recall of device recall is the process of removing a product from the market due to safety concerns.
Who is required to file recall of device recall?
Manufacturers, distributors, and retailers are required to file recall of device recall.
How to fill out recall of device recall?
To fill out recall of device recall, the company must provide information about the product, reason for the recall, and actions taken to address the issue.
What is the purpose of recall of device recall?
The purpose of recall of device recall is to protect consumers from harmful products and ensure public safety.
What information must be reported on recall of device recall?
Information such as product details, hazard description, number of units affected, and corrective actions must be reported on recall of device recall.
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