# FDA recall Z-2439-2019

> **Becton Dickinson & Co.** · Class II · device recall initiated 2019-07-26.

## Product

BD Kiestra InoqulA+ Software Version 20.3. IVD automated specimen processing     Catalog Number : 447213

## Reason for recall

An anomaly is present in InoqulA / InoqulA+ software version 20.3, has the potential to cause a mismatch between a specimen and plate

## Distribution

Illinois, Iowa, Missouri, New York, Ohio, Tennessee  World Wide (5): Singapore, Taiwan, France, Netherlands

## Key facts

- **Recall number:** Z-2439-2019
- **Recalling firm:** Becton Dickinson & Co.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-07-26
- **Report date:** 2019-09-11
- **Termination date:** 2019-12-06

- **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-2439-2019

## Citation

> AI Analytics. FDA recall Z-2439-2019. Retrieved 2026-06-09 from https://api.ai-analytics.org/recall/Z-2439-2019. Source: US FDA. Licensed CC0.

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