# FDA recall Z-2470-2023

> **Skytron, LLC** · Class II · device recall initiated 2023-08-01.

## Product

GS70H Salus Surgical Table, Product Code 18-071-70

## Reason for recall

When the control of the operating table was used in Bluetooth mode, the operating table continued moving even after releasing the button on the control.    Originally, the root cause was thought to be confined to Bluetooth/wireless communications between the control pendant and the surgical table. However, during investigation, Mizuho discovered that the failure could be replicated even in wired mode if communication between the pendant and table were somehow interrupted. The root cause appears to be: if communication between the controller and table is interrupted while a button is pressed, the table does not know if/when a button is released. This occurs in wireless or wired mode.

## Distribution

Worldwide - US Nationwide distribution in the states of AL, AR, CA, CT, FL, GA, IA, IL, IN, MA, MI, MO, PA, TN, TX, UT, WA, WI and the countries of  Australia, New Zealand.

## Key facts

- **Recall number:** Z-2470-2023
- **Recalling firm:** Skytron, LLC
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2023-08-01
- **Report date:** 2023-09-06

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Grand Rapids, MI, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2470-2023

## Citation

> AI Analytics. FDA recall Z-2470-2023. Retrieved 2026-07-01 from https://api.ai-analytics.org/recall/Z-2470-2023. Source: US FDA. Licensed CC0.

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