# FDA recall Z-2420-2025

> **MAQUET GMBH** · Class II · device recall initiated 2025-07-14.

## Product

Corin Operating Tables  Model Numbers: (1) 770001A0, (2) 770001A2, (3) 770001B0, (4) 770001B2, (5) 770001F0, (6) 770001F2;  All Software Versions.

## Reason for recall

Under certain conditions, such as the simultaneous use of the operating table with other medical devices, including high-frequency (HF) surgical equipment, interference may occur that could prevent the device from performing as intended. If the issue occurs, the operating table is unresponsive to command from both the universal remote control and override panel.

## Distribution

Worldwide - US Nationwide distribution in the states of KY, NY, TX and the countries of  Algeria, Australia, Austria, Bulgaria, Canada, China, Colombia, Denmark, Egypt, Estonia, Finland, France, Germany, Ireland, Israel, Italy, Japan, Jordan, Korea, Republic of, Kuwait, Lebanon, Morocco, Netherlands, Norway, Poland, Portugal, Romania, Saudi Arabia, Singapore, South Africa, Spain, Sweden, Switzerland, Thailand, Turkey, United Arab Emirates, United Kingdom.

## Key facts

- **Recall number:** Z-2420-2025
- **Recalling firm:** MAQUET GMBH
- **Classification:** Class II
- **Product type:** device
- **Status:** Ongoing
- **Initiation date:** 2025-07-14
- **Report date:** 2025-09-03

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Rastatt, Germany

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-2420-2025

## Citation

> AI Analytics. FDA recall Z-2420-2025. Retrieved 2026-08-18 from https://api.ai-analytics.org/recall/Z-2420-2025. Source: US FDA. Licensed CC0.

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