PlainRecalls
FDA Devices Moderate Class II Terminated

3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573

Reported: July 31, 2019 Initiated: February 1, 2019 #Z-2007-2019

Product Description

3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573

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.

Details

Units Affected
460,800
Distribution
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.
Location
Franklin Lakes, NJ

Frequently Asked Questions

What product was recalled?
3mL Luer-Lok Syringe, Catalog Number 309657, UDI 30382903096573. Recalled by Becton Dickinson & Company. Units affected: 460,800.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on July 31, 2019. Severity: Moderate. Recall number: Z-2007-2019.