Potential for the lid of the catheter connector to be in the incorrect position.
Reason for recall: Potential for the lid of the catheter connector to be in the incorrect position. Distribution: Nationwide distribution to AK, AL, AR, AZ, CA, CO, FL, GA, HI, IA, IL, IN, KS, LA, MA, MD, ME, MI, MN, MO, MS, NC, NE, NJ, NM, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV. Quantity: 60 units Lot/code info: REF: 530185; Product Code: SESK; UDI-DI (Primary): 04046955625147; UDI-DI (Unit of Use): 04046955625130; Lot Number: 0062003227. Expiration Date: 07/31/2026.
04046955625147, 04046955625130
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.