FDA recall Z-2008-2019

Becton Dickinson & Company · Class II · device

Product

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

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.

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.

Key facts

Status
Terminated
Initiation date
2019-02-01
Report date
2019-07-31
Termination date
2020-06-11
Voluntary/Mandated
Voluntary: Firm initiated
Location
Franklin Lakes, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2008-2019