Medical device recalls Moderate risk

Becton Dickinson & Company recalls 3mL Safety-Lok Syringe, Catalog Number 309606, UDI 30382903096061

Recall date
February 1, 2019
Source
U.S. Food & Drug Administration (FDA) — enforcement report
Recall number
Z-2008-2019
FDA classification
Class II
Brand / firm
Becton Dickinson & Company
Sold / distributed
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.

Why it was 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.

Class II means using this product may cause temporary or medically reversible health problems; the chance of serious harm is remote.

What was recalled

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

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