Becton Dickinson & Company: Medical Device Recall in 2019 - (Recall #: Z-0500-2020)

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 Posiflush Pre-Filled Normal Saline Syringes Catalog Number: 306575 (Canada only)

Product Classification:

Class II

Date Initiated: October 14, 2019

Date Posted: November 27, 2019

Recall Number: Z-0500-2020

Event ID: 84113

Reason for Recall:

Limited number of syringes labeled Posiflush Experimental Product and Not for Human Use being mixed with standard BD Posiflush Pre-Filled Normal Saline Syringes.

Status: Terminated

Product Quantity: 967,680

Code Information:

Lot Number: 9175971 UDI: 50382903065757

Distribution Pattern:

Distribution US Nationwide and Canada

Voluntary or Mandated:

Voluntary: Firm initiated