# FDA recall Z-0095-2023

> **Becton Dickinson & Company** · Class II · device recall initiated 2022-09-15.

## Product

BD Vacutainer Tube Sodium Fluoride: 100 mg, Potassium Oxalate: 20 mg, Catalog Number 367001. For collecting, transporting, separating, and processing blood for blood alcohol determination.

## Reason for recall

The affected product contains isobutylene which has recently demonstrated potential interference in determination of methanol by gas chromatography methods. The interference may lead to false positive results in methanol testing.

## Distribution

Distribution US nationwide, Canada, New Zealand, and Hong Kong.

## Key facts

- **Recall number:** Z-0095-2023
- **Recalling firm:** Becton Dickinson & Company
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-09-15
- **Report date:** 2022-10-26

- **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-0095-2023

## Citation

> AI Analytics. FDA recall Z-0095-2023. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0095-2023. Source: US FDA. Licensed CC0.

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