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TemplateData for Admin recall notice This template is used to notify an administrator that a recall petition has been opened under the administrator recall policy. The above documentation is transcluded from Template:Admin recall notice/doc .
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See a monthly parameter usage report for Template:Admin recall notice/AN in articles based on its TemplateData. TemplateData for Admin recall notice/AN This template is used to notify the Administrators' noticeboard that a recall petition has been opened for an administrator under the administrator recall policy.
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The recall process described here proceeds in two stages, petition and re-confirmation. In the petition stage, editors ask an admin to stand for re-confirmation or resign. If the petition meets an initial threshold, it triggers the re-confirmation stage, in which editors decide whether the user is to retain adminship.
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FDA's role under the guidelines is to monitor company recalls and assess the adequacy of a firm's action. After a recall is completed, FDA makes sure that the product is destroyed or suitably reconditioned and investigates why the product was defective. Generally, FDA accepts reports and other necessary recall information submitted by e-mail.
The standard test involves the recall period starting immediately after the final list item; this can be referred to as immediate free recall (IFR) to distinguish it from delayed free recall (DFR). In delayed free recall, there is a short distraction period between the final list item and the start of the recall period.