Fujifilm FDR Go Plus mobile X-ray system — Class II medical device recall Z-2441-2019
Terminated recall by Fujifilm Medical Systems U.S.A., Inc., reported 2019-09-11, distributed nationwide. The graphics driver of the FDR Go PLUS might cause the appearance of a Blue Screen of Death (BSoD)
| Recall number | Z-2441-2019 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Fujifilm Medical Systems U.S.A., Inc., Lexington, MA, United States |
| Recall initiated | 2019-07-19 |
| Classified | 2019-08-30 |
| Reported by FDA | 2019-09-11 |
| Terminated | 2020-08-28 |
| Distributed | Nationwide (US) |
| Quantity | 174 units |
Product
Fujifilm FDR Go Plus mobile X-ray system
Reason for recall
The graphics driver of the FDR Go PLUS might cause the appearance of a Blue Screen of Death (BSoD)
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-2441-2019. 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.