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Becton Dickinson & Company recalls BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog
Recalled June 12, 2019 · FDA recall Z-1710-2019 · Becton Dickinson &
Hazard
Leak from the septum assembly or the canister may burst under high pressure which could result in blood exposure to a health care worker. · FDA Class II
Units
6,720 units
Sold at
US distribution to one distributor in VA.
Description
Leak from the septum assembly or the canister may burst under high pressure which could result in blood exposure to a health care worker.
Product
BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog Number: 383536
Manufacturer(s)
Becton Dickinson & Company
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →