# FDA recall Z-0526-2022

> **NRT X-RAY A/S** · Class II · device recall initiated 2022-01-21.

## Product

1. Footrest ( use exclusively in combination with Intelli-C devices)  2. Shoulder support ( use exclusively in combination with Intelli-C devices)

## Reason for recall

Friction rubber block in the clamping mechanism was missing in the Footrest. It may slip down along the patient table while in use with a patient. This accessory is designed to use with Intelli-C, Right and Intelli-C, Left.

## Distribution

USA: IA, KY,LA, MA, NC,NY, OH, SC, WA, WV      OUS: Switzerland, Czech Republic, Germany, Denmark, Netherlands, RSA, Sweden

## Key facts

- **Recall number:** Z-0526-2022
- **Recalling firm:** NRT X-RAY A/S
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2022-01-21
- **Report date:** 2022-02-02

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

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0526-2022

## Citation

> AI Analytics. FDA recall Z-0526-2022. Retrieved 2026-07-18 from https://api.ai-analytics.org/recall/Z-0526-2022. Source: US FDA. Licensed CC0.

---

*[Dataset catalog](/datasets/) · [FDA recalls dataset](/datasets/fda-recalls) · CC0 1.0*