# FDA recall Z-2750-2017

> **Becton Dickinson & Company** · Class II · device recall initiated 2016-09-16.

## Product

BD 3ml Syringe Luer-Lok" Tip with BD PrecisionGlide" Needle 18G x 1 1/2 (1.2mm x 40mm)  Catalog #309580  The BD Single Use, Hypodermic Syringe is intended for use by health care professionals for general purpose fluid aspiration/injection

## Reason for recall

BD identified that several lots did not receive the specified dose of irradiation necessary to meet the Sterility Assurance Level (SAL) required.

## Distribution

Nationwide Distribution

## Key facts

- **Recall number:** Z-2750-2017
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2016-09-16
- **Report date:** 2017-07-26
- **Termination date:** 2018-03-20

- **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-2750-2017

## Citation

> AI Analytics. FDA recall Z-2750-2017. Retrieved 2026-06-04 from https://api.ai-analytics.org/recall/Z-2750-2017. Source: US FDA. Licensed CC0.

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