# FDA recall Z-2361-2020

> **Abaxis Inc** · Class II · device recall initiated 2019-12-11.

## Product

Piccolo Xpress chemistry analyzer, Model No. 1100-1001, Software version 2.1.55 (NGA)/3.1.35(Jen II)

## Reason for recall

Incorrect reference ranges of analytes.

## Distribution

All U.S. Consignees, TX, PA, FL, OK, KY, CA, VA  No OUS Consignees.

## Key facts

- **Recall number:** Z-2361-2020
- **Recalling firm:** Abaxis Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-12-11
- **Report date:** 2020-06-24
- **Termination date:** 2022-07-22

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Union City, CA, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2361-2020

## Citation

> AI Analytics. FDA recall Z-2361-2020. Retrieved 2026-07-04 from https://api.ai-analytics.org/recall/Z-2361-2020. Source: US FDA. Licensed CC0.

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