Home / Recalls / Medical Devices
Becton Dickinson & Company recalls BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (OUS)
Recalled July 27, 2022 · FDA recall Z-1438-2022 · Becton Dickinson &
Hazard
May have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate and biohazardous material, under dosing/under infusion, contamination and/or air ingress. · FDA Class II
Units
448,040
Sold at
Worldwide distribution - US Nationwide distribution in the states of AK, AR, AZ, CA, CO, FL, GA, IL, IN, KS, MA, MD, MI, MN, MO, MS, NC, NE, NJ, NV, NY, OH, OR, PA, SD, TN, TX, UT, VA, WA, WV and the countries of Belgium, China, India, Indonesia, Japan, Korea, Nepal, Philippines, Singapore, Sri Lanka, Thailand, Vietnam.
Description
May have the potential for leakage at the housing component of the stopcock, may result in delay or interruption in treatment, exposure to infusate and biohazardous material, under dosing/under infusion, contamination and/or air ingress.
Product
BD Connecta White 360 Shelf 100Ea Catalog No. 395000 (OUS)
Manufacturer(s)
Becton Dickinson & Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →