# FDA recall Z-0492-2018

> **Tosoh Bioscience Inc** · Class II · device recall initiated 2017-06-11.

## Product

Tosoh¿Sorter 9tray, Product Code 022931and Tosoh¿Sorter 19tray, Product Code 022932.    Product Usage:  The AIA-900 9tray Sorter and AIA-900 19tray Sorter supports the automation of the AIA-900 systems.

## Reason for recall

This recall has been initiated due to a potential malfunction of the photo interrupter (Pl). The potential  malfunction has been attributed to aging and premature deterioration of the Pl collector current.

## Distribution

Worldwide Distribution - U.S. Nationwide - Latin America

## Key facts

- **Recall number:** Z-0492-2018
- **Recalling firm:** Tosoh Bioscience Inc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2017-06-11
- **Report date:** 2018-02-07
- **Termination date:** 2019-12-31

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Grove City, OH, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0492-2018

## Citation

> AI Analytics. FDA recall Z-0492-2018. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-0492-2018. Source: US FDA. Licensed CC0.

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