Class II — NRT X-RAY A/S
| Recalling firm | NRT X-RAY A/S |
|---|---|
| Registered facility | NRT X-RAY A/S (the firm's only registered facility) |
| Classification | Class II |
| Status | Ongoing |
| Reason | There is a potential that the drive shaft in the detector up/down (IDE) movement of the X-Ray machine may break which causes the detector to move until it is stopped by the movement end-stop. |
| Product | Intelli-C, Right side suspended Tabletop, REF: 03400000 |
| Quantity | 32 units |
| Distribution | US Nationwide distribution in the states of OH, NC, KY, SC, IA, MA, WA, LA, NV, NY. |
| Initiated | 2023-04-27 |
| Classified | 2023-05-31 |
| Recall number | Z-1668-2023 |
| 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 — NRT X-RAY A/S (Z-1668-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/92230/
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