# FDA recall Z-0630-2022

> **Becton Dickinson & Co.** · Class II · device recall initiated 2022-01-05.

## Product

BD Veritor Plus Analyzer - intended to provide rapid test results in near-patient settings.   Catalog Number: 256066

## Reason for recall

May have the potential to overheat and/or cause fire,   the issue can occur when an unauthorized alternative AC power adapter, and not the one provided by BD is used to power the instrument.

## Distribution

Worldwide distribution - US Nationwide and the countries of Armenia, Australia, Belgium, Brazil, Canada, Chile, China, Colombia, Dominican Republic, Ecuador, Fiji, Guatemala, Hong Kong, Honduras, Haiti, Indonesia, India, Jamaica, Cambodia, South Korea, Macao, Mexico, New Zealand, Panama, Peru, Philippines, Singapore, El Salvador, Thailand, Trinidad and Tobago, Taiwan, Uruguay, Vietnam.

## Key facts

- **Recall number:** Z-0630-2022
- **Recalling firm:** Becton Dickinson & Co.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-01-05
- **Report date:** 2022-02-16

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Sparks, MD, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0630-2022

## Citation

> AI Analytics. FDA recall Z-0630-2022. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0630-2022. Source: US FDA. Licensed CC0.

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