Becton Dickinson & Company: Medical Device Recall in 2020 - (Recall #: Z-0125-2021)

Updated on March 25, 2026.

See the recall detail below. You can also see other recalls from the same firm in 2020.

Data Source: FDA.

Product Description:

BD Nexiva Closed IV Catheter System Dual Port (20 GA 1.75 IN) Catalog (Ref) No. 383538 BD Nexiva closed IV catheter systems are intended to be inserted into a patient s vascular system for short term use to sample blood, monitor blood pressure, or administer fluids.

Product Classification:

Class II

Date Initiated: September 14, 2020

Date Posted: October 28, 2020

Recall Number: Z-0125-2021

Event ID: 86434

Reason for Recall:

Dull/blunt needles within the IV Catheter System may lead to missed insertion attempts and delay in diagnosis or treatment until a new needle is inserted

Status: Terminated

Product Quantity: 12,020 units

Code Information:

Lot Number: 9325212 UDI: 30382903835387

Distribution Pattern:

US: Nationwide Distribution: AK, AR, AZ, CA, IL, KS, MO, NY, OH, UT, VA; and International to: Canada and Mexico.

Voluntary or Mandated:

Voluntary: Firm initiated