# FDA recall Z-1313-2019

> **Becton Dickinson & Co.** · Class II · device recall initiated 2019-04-03.

## Product

BD Veritor Plus Analyzer- In-Vitro Diagnostic  intended to use with the BD Veritor System Test Devices.  Catalog Number: 256066

## Reason for recall

Background calibration has the potential to cause false positive or false negative test results. An incorrect test result with the BD Veritor System could lead to possible misdiagnosis and inappropriate treatment

## Distribution

Nationwide  Foreign:  Canada, Chile, Hong Kong, Japan, Taiwan

## Key facts

- **Recall number:** Z-1313-2019
- **Recalling firm:** Becton Dickinson & Co.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-04-03
- **Report date:** 2019-05-22
- **Termination date:** 2020-05-04

- **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-1313-2019

## Citation

> AI Analytics. FDA recall Z-1313-2019. Retrieved 2026-06-03 from https://api.ai-analytics.org/recall/Z-1313-2019. Source: US FDA. Licensed CC0.

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