# FDA recall Z-0209-2022

> **Zhejiang Kindly Medical Devices Co., Ltd.** · Class II · device recall initiated 2021-08-24.

## Product

HENRY SCHEIN Safety Blood Collection Needle 22Gx 1 1/4 Inch, REF 570-2068, 100pcs/box 1000pcs/ctn 350*210*350mm

## Reason for recall

Potential for difficulty in safety mechanism activation.

## Distribution

U.S. Nationwide distribution.

## Key facts

- **Recall number:** Z-0209-2022
- **Recalling firm:** Zhejiang Kindly Medical Devices Co., Ltd.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2021-08-24
- **Report date:** 2021-11-17
- **Termination date:** 2023-07-21

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Wenzhou, N/A, China

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0209-2022

## Citation

> AI Analytics. FDA recall Z-0209-2022. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-0209-2022. Source: US FDA. Licensed CC0.

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