FDA recall Z-1710-2019

Becton Dickinson & Company · Class II · device

Product

BD Nexiva Dual Port 20GA 1.00IN -Closed IV Catheter System intended for use in the peripheral vascular system Catalog Number: 383536

Reason for recall

Leak from the septum assembly or the canister may burst under high pressure which could result in blood exposure to a health care worker.

Distribution

US distribution to one distributor in VA.

Key facts

Status
Terminated
Initiation date
2019-03-01
Report date
2019-06-12
Termination date
2020-05-21
Voluntary/Mandated
Voluntary: Firm initiated
Location
Franklin Lakes, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1710-2019