# FDA recall Z-2008-2019

> **Becton Dickinson & Company** · Class II · device recall initiated 2019-02-01.

## 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

- **Recall number:** Z-2008-2019
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **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

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

## Citation

> AI Analytics. FDA recall Z-2008-2019. Retrieved 2026-06-01 from https://api.ai-analytics.org/recall/Z-2008-2019. Source: US FDA. Licensed CC0.

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