Class II — GE Healthcare, LLC
| Recalling firm | GE HealthCare Technologies Inc. |
|---|---|
| Registered facility | View this company's 50 registered facilities → (openFDA recall records do not name a specific facility) |
| Classification | Class II |
| Status | Terminated |
| Reason | An unexpected column motion while attempting to park the column on the AMX Navigate mobile X-ray system. |
| Product | AMX Navigate Mobile X-Ray System |
| Quantity | 3 units |
| Distribution | Domestic Distribution Only |
| Initiated | 2021-06-24 |
| Classified | 2021-09-29 |
| Terminated | 2023-06-14 |
| Recall number | Z-2590-2021 |
| Initiation | Voluntary: Firm initiated |
Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)
Cite this record
RegWarden. “Class II recall — GE Healthcare, LLC (Z-2590-2021).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/88601/
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