# FDA recall Z-2251-2020

> **Abbott Laboratories** · Class II · device recall initiated 2020-04-02.

## Product

Accelerator APS Aliquoter Module, List number: 07L40 - Product Usage: The ACCELERATOR APS Workcell is a modular system designed to automate sample handling and processing in the clinical laboratory. The system allows consolidations of multiple clinical chemistry and immunoassay analytical instruments into a unified workstation.

## Reason for recall

In the case of an AQM clot detection error a portion of the distilled water from the Aliquoter Module hydraulic circuit may be dispensed into the Primary Tube leading to sample dilution, which could lead to incorrect results.

## Distribution

Worldwide distribution - U.S. Nationwide distribution including in the states of  NC, ND, SC, TN.    The countries of  United Kingdom, France, New Zealand, Pakistan, Turkey.

## Key facts

- **Recall number:** Z-2251-2020
- **Recalling firm:** Abbott Laboratories
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-04-02
- **Report date:** 2020-06-10
- **Termination date:** 2021-04-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Irving, TX, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2251-2020

## Citation

> AI Analytics. FDA recall Z-2251-2020. Retrieved 2026-07-20 from https://api.ai-analytics.org/recall/Z-2251-2020. Source: US FDA. Licensed CC0.

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