Class II — UIH Technologies LLC
| Recalling firm | UIH Technologies LLC |
|---|---|
| Registered facility | UIH TECHNOLOGIES, LLC (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | Third-party outer covers can become trapped between patient table and gantry, causing mechanical interference during table movement. |
| Product | Shanghai United Imaging Healthcare Co., Ltd. Computed Tomography X-ray System, Model:uCT 550 MD, Rx Only |
| Quantity | 22 units |
| Distribution | US: OUS: |
| Initiated | 2025-09-12 |
| Classified | 2025-10-21 |
| Recall number | Z-0218-2026 |
| 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 — UIH Technologies LLC (Z-0218-2026).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/97668/
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