Tosoh¿Sorter 9tray — Class II medical device recall Z-0492-2018
Terminated recall by Tosoh Bioscience Inc, reported 2018-02-07, distributed nationwide. This recall has been initiated due to a potential malfunction of the photo interrupter (Pl). The potential mal
| Recall number | Z-0492-2018 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Tosoh Bioscience Inc, Grove City, OH, United States |
| Recall initiated | 2017-06-11 |
| Classified | 2018-01-30 |
| Reported by FDA | 2018-02-07 |
| Terminated | 2019-12-31 |
| Distributed | Nationwide (US) |
| Quantity | 565 devices |
| Reason classes | device malfunction |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0492-2018. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.