Toshiba Ultra-Short Magnetic Resonance Imaging System — Class II medical device recall Z-2315-2012
Terminated recall by Toshiba American Medical Systems Inc, reported 2012-09-12, distributed nationwide. The firm recalled due to a potentail problem with the position of the hold in the lug teminals on the power ca
| Recall number | Z-2315-2012 |
|---|---|
| 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 | 2012-02-21 |
| Classified | 2012-09-06 |
| Reported by FDA | 2012-09-12 |
| Terminated | 2012-09-07 |
| Distributed | Nationwide (US) |
| Quantity | 3 units |
| Serial numbers | P3F11Z2143, P5A0632002, P5B06Y2005, P5B0712006 |
Product
Toshiba Ultra-Short Magnetic Resonance Imaging System, EXCELART Vantage. MRT-1503/P5-Vantage MRI System. MR imaging.
Reason for recall
The firm recalled due to a potentail problem with the position of the hold in the lug teminals on the power cables connected to the terminal blocks on the gradient coil.
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-2315-2012. 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.