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URGENT: MEDICAL DEVICE RECALL Epic Suction Irrigation Reusable ProbeCustomer Name Hospital Name Street Address City, State, Zip Code Affected Product: Epic Suction Irrigation Reusable Probe 10 January
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01
Gather all the necessary information regarding the saline product being recalled.
02
Follow the instructions provided in the recall notice or form.
03
Fill out the recall form completely and accurately, providing all requested information.
04
Include any relevant documentation or proof of purchase if required.
05
Submit the completed recall form according to the instructions provided.

Who needs recall of certain saline?

01
Individuals who have purchased or used the specified saline product being recalled.
02
Healthcare providers who have distributed or prescribed the recalled saline product to patients.
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Recall of certain saline refers to the process of withdrawing a specific lot or batch of saline solution from the market due to safety concerns, contamination, or failure to meet quality standards.
Manufacturers and distributors of saline products are required to file a recall of certain saline if they determine that their product poses a risk to public health.
To fill out a recall of certain saline, manufacturers should complete the designated recall reporting form provided by regulatory agencies, detailing the product information, reason for recall, and distribution details.
The purpose of recall of certain saline is to protect public health by removing potentially harmful products from circulation and informing consumers about the risks associated with the affected products.
The report must include product details (name, lot number, expiration date), reason for the recall, quantity affected, distribution channels, and measures taken to notify customers.
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