Numb regulates endocytosis in many metazoans, but the mechanism by which it functions is not completely understood. Here we report that the Caenorhabditis elegans Numb ortholog, NUM‐1A, a regulator of endocytic recycling, binds the C isoform of transbilayer amphipath transporter‐1 (TAT‐1), a P4 family adenosine triphosphatase and putative aminophospholipid translocase that is required for proper endocytic trafficking. We demonstrate that TAT‐1 is differentially spliced during development and that TAT‐1C‐specific splicing occurs in the intestine where NUM‐1A is known to function. NUM‐1A and TAT‐1C colocalize in vivo. We have mapped the binding site to an NXXF motif in TAT‐1C. This motif is not required for TAT‐1C function but is required for NUM‐1A's ability to inhibit recycling. We demonstrate that num‐1A and tat‐1 defects are both suppressed by the loss of the activity of PSSY‐1, a phosphatidylserine (PS) synthase. PS is mislocalized in intestinal cells with defects in tat‐1 or num‐1A function. We propose that NUM‐1A inhibits recycling by inhibiting TAT‐1C's ability to translocate PS across the membranes of recycling endosomes.