Home / Recalls / Medical Devices
Bard Peripheral Vascular Inc recalls EQUISTREAM¿ XK Long-Term Hemodialysis Catheter. REF/UDI:5913190/(01)00801741013836; 16F
Recalled June 10, 2020 · FDA recall Z-2209-2020 · Bard Peripheral Vascular
Hazard
Incorrect Peel-Apart Introducer Sheath in Kit. · FDA Class II
Units
400
Sold at
67 US Consignees. US - AL, AR, AZ, CA, FL, GA, IA, ID, IL, KY, LA, MD, MN, MT, NC, NY, OR, PA, TN, TX, VA, WA, WI and WV.
Description
Incorrect Peel-Apart Introducer Sheath in Kit.
Product
EQUISTREAM¿ XK Long-Term Hemodialysis Catheter. REF/UDI:5913190/(01)00801741013836; 16F
Manufacturer(s)
Bard Peripheral Vascular Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →