# FDA recall Z-1210-2019

> **Becton Dickinson & Company** · Class I · device recall initiated 2019-02-28.

## Product

SmartSite Syringe Administration Set-Product Package Size 50,   Catalog Number: 10798696

## Reason for recall

Leaking of the Smartsite Syringe Administration Set.  May result in delay or interruption of infusion, under-infusion, contamination of the fluid path and HCP exposure to infusates.

## Distribution

US Nationwide Distribution in the states of AR, NH, NC

## Key facts

- **Recall number:** Z-1210-2019
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class I
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-02-28
- **Report date:** 2019-07-03
- **Termination date:** 2020-07-30

- **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-1210-2019

## Citation

> AI Analytics. FDA recall Z-1210-2019. Retrieved 2026-06-05 from https://api.ai-analytics.org/recall/Z-1210-2019. Source: US FDA. Licensed CC0.

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