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: 0 units Lot/code info: REF: 332078; Product Code: CE17TKFCPS; UDI-DI (Primary): 04046955899432; UDI-DI (Unit of Use): 04046955899449; Lot Numbers: 0062006314, 0062011670, 0062028428. Expiration Date: 07/31/2026
04046955899432, 04046955899449
Official record: FDA (Device enforcement) ↗
Republished from the official source above; details can change — the source record controls.