Becton Dickinson & Company: Medical Device Recall in 2019 - (Recall #: Z-1710-2019)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2019.

Data Source: FDA.

Product Description:

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

Product Classification:

Class II

Date Initiated: March 1, 2019

Date Posted: June 12, 2019

Recall Number: Z-1710-2019

Event ID: 82330

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.

Status: Terminated

Product Quantity: 6,720 units

Code Information:

Lot Number: 8337721 Exp. 30-Nov-2021 UDI: 382903835362

Distribution Pattern:

US distribution to one distributor in VA.

Voluntary or Mandated:

Voluntary: Firm initiated