# FDA recall Z-1663-2025

> **IHB OPERATIONS B.V.** · Class II · device recall initiated 2025-03-27.

## Product

Skytron Freedom 4FXS-60 Heavy Duty Monitor Mount

## Reason for recall

The mounting hardware that is supplied with the 4FXS-60 monitor bracket does not provide adequate thread engagement to support the weight of the frame and monitor. This could lead to a failure of the mounting hardware and subsequent separation of the frame from the mounting column.

## Distribution

US Nationwide distribution including in the states of AL, AZ, CA, FL, IA, ID, IL, LA, MA, MD, MI, MN, NC, NH, NJ, NM, NY, PA, TN, TX, UT, VA, WI, WV.

## Key facts

- **Recall number:** Z-1663-2025
- **Recalling firm:** IHB OPERATIONS B.V.
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-03-27
- **Report date:** 2025-04-30

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Zwolle, N/A, Netherlands

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-1663-2025

## Citation

> AI Analytics. FDA recall Z-1663-2025. Retrieved 2026-05-27 from https://api.ai-analytics.org/recall/Z-1663-2025. Source: US FDA. Licensed CC0.

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