Becton Dickinson & Company: Medical Device Recall in 2019 - (Recall #: Z-2008-2019)

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:

3mL Safety-Lok Syringe, Catalog Number 309606, UDI 30382903096061

Product Classification:

Class II

Date Initiated: February 1, 2019

Date Posted: July 31, 2019

Recall Number: Z-2008-2019

Event ID: 82138

Reason for Recall:

The syringes have scale markings that were printed incorrectly. The scale is skewed to varying degrees, resulting in missing and/or partially printed scale numbers and scale lines.

Status: Terminated

Product Quantity: 428,800

Code Information:

Lot Number 8307694

Distribution Pattern:

The products were distributed to the following US states: FL, IL, KS, MA, ND, NH, NY, OH, PA, RI, SC, VA, and WI. The products were distributed to the following foreign countries: Suriname.

Voluntary or Mandated:

Voluntary: Firm initiated