# FDA recall Z-1109-2021

> **Becton Dickinson & Company** · Class II · device recall initiated 2020-12-23.

## Product

BD Hypodermic Syringe 10 ml, eccentric tip.  Catalog (Ref No.) 305482

## Reason for recall

The product packaging for the 10 ml eccentric tip syringe may exhibit open seals.  An open seal impacts package integrity and potentially compromises sterility of the syringe.

## Distribution

Distribution US nationwide and Canada

## Key facts

- **Recall number:** Z-1109-2021
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-12-23
- **Report date:** 2021-02-24
- **Termination date:** 2022-11-21

- **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-1109-2021

## Citation

> AI Analytics. FDA recall Z-1109-2021. Retrieved 2026-07-16 from https://api.ai-analytics.org/recall/Z-1109-2021. Source: US FDA. Licensed CC0.

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