# FDA recall Z-0207-2018

> **Becton Dickinson & Company** · Class II · device recall initiated 2017-05-31.

## Product

BD Precision Glide Needle 18G x 1  RB, Catalog 305195    Product Usage:  These needles are intended for general purpose fluid injection/aspiration, infusion, venipuncture to obtain blood collection and insulin injection.

## Reason for recall

Hub damage resulting in breakage and/or leakage during use.

## Distribution

Nationwide Distribution

## Key facts

- **Recall number:** Z-0207-2018
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-05-31
- **Report date:** 2017-12-13
- **Termination date:** 2018-06-28

- **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-0207-2018

## Citation

> AI Analytics. FDA recall Z-0207-2018. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0207-2018. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*