# FDA recall Z-0252-2020

> **Becton Dickinson & Company** · Class II · device recall initiated 2019-03-07.

## Product

BD Vacutainer Eclipse Blood Collection Needles 22Gx1.25, cat. no. 368608

## Reason for recall

BD PAS received customer complaints indicating the absence of the bevel on the non-patient needle end of the product, causing blood leakage.

## Distribution

Distributed to accounts in AR, CT, FL, IL, IN, MI, MO, MS, NY, OH, TN, TX, and VA. Foreign distribution to Canada, Brazil, India, Mexico, Singapore, and Taiwan.

## Key facts

- **Recall number:** Z-0252-2020
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-03-07
- **Report date:** 2019-11-06
- **Termination date:** 2022-02-11

- **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-0252-2020

## Citation

> AI Analytics. FDA recall Z-0252-2020. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0252-2020. Source: US FDA. Licensed CC0.

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