When a recall is in edit mode, the Recall Coordinator can add additional information, products, or locations as is appropriate.
A notification will need to be resent for any active locations to receive the changes.
Material Changes
Material changes to the recall include changes to the FDA classification, additional patient risk, additional documents or products. These changes typically go to all locations impacted by the recall event. To make these changes
1. Click the Edit Recall button.
2. Make changes to Event Details, Description, Add Documents, Add/Change Actions, Add Products.
3. Resend the Notification.
Logging Changes
After any changes are made to an active recall event, the system will prompt the user to log the changes.
It is a best practice to keep a log of any changes made to an active recall. The log can be viewed under the Change History tab.
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