# FDA recall Z-1668-2023

> **NRT X-RAY A/S** · Class II · device recall initiated 2023-04-27.

## Product

Intelli-C, Right side suspended Tabletop, REF: 03400000

## Reason for recall

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.

## Distribution

US Nationwide distribution in the states of OH, NC, KY, SC, IA, MA, WA, LA, NV, NY.

## Key facts

- **Recall number:** Z-1668-2023
- **Recalling firm:** NRT X-RAY A/S
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-04-27
- **Report date:** 2023-06-07

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Hasselager, N/A, Denmark

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1668-2023

## Citation

> AI Analytics. FDA recall Z-1668-2023. Retrieved 2026-06-24 from https://api.ai-analytics.org/recall/Z-1668-2023. Source: US FDA. Licensed CC0.

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