# FDA recall Z-0084-2018

> **Becton Dickinson & Company** · Class II · device recall initiated 2017-01-27.

## Product

BD Vacutainer Sodium Polyanetholesulfonate 5.95 mg Sodium Chloride 14.4 mg Blood Collection Tubes for Microbiological Studies (8.3 mL * 16x100mm) Catalog No. 364960

## Reason for recall

After a receiving a customer complaint for incorrect labeling, BD has confirmed that a portion of SPS tubes associated with catalog 364960, lot 6090812 were incorrectly labeled at the case and shelf pack level.

## Distribution

Nationwide, Canada

## Key facts

- **Recall number:** Z-0084-2018
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-01-27
- **Report date:** 2017-11-15
- **Termination date:** 2019-02-06

- **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-0084-2018

## Citation

> AI Analytics. FDA recall Z-0084-2018. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-0084-2018. Source: US FDA. Licensed CC0.

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