Toshiba Aquilion CT System TSX-303A — Class II medical device recall Z-0018-2016
Terminated recall by Toshiba American Medical Systems Inc, reported 2015-10-21, distributed in PR. If two specific operations are performed in multi-phase helical scanning, the acquired raw data may not be sav
| Recall number | Z-0018-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Toshiba American Medical Systems Inc, Tustin, CA, United States |
| Recall initiated | 2015-05-08 |
| Classified | 2015-10-09 |
| Reported by FDA | 2015-10-21 |
| Terminated | 2016-10-26 |
| Distributed | PR |
| Quantity | 459 |
Product
Toshiba Aquilion CT System TSX-303A
Reason for recall
If two specific operations are performed in multi-phase helical scanning, the acquired raw data may not be saved.
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-0018-2016. 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.