# FDA recall Z-0710-2022

> **Abbott Molecular, Inc.** · Class II · device recall initiated 2022-02-11.

## Product

Alinity m Integrated Reaction Units (IRU)

## Reason for recall

There is potential for the Reaction Vessels (RVs) detaching from the RV cap during transport by the pipettor robot.

## Distribution

US Nationwide distribution in the states of AZ, CA, CO, CT, DC, FL, GA, IL, KY, LA, MA, MI, MO, NC, NJ, NY, OK, RI, SD, TX, WA, and WI.

## Key facts

- **Recall number:** Z-0710-2022
- **Recalling firm:** Abbott Molecular, Inc.
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2022-02-11
- **Report date:** 2022-03-09
- **Termination date:** 2023-04-14

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Des Plaines, IL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0710-2022

## Citation

> AI Analytics. FDA recall Z-0710-2022. Retrieved 2026-06-25 from https://api.ai-analytics.org/recall/Z-0710-2022. Source: US FDA. Licensed CC0.

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*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*
