# FDA recall Z-0133-2021

> **Maquet Cardiovascular Us Sales, Llc** · Class II · device recall initiated 2020-09-24.

## Product

Yuno II Mobile Operating Table - Product Usage: support and position the patient immediately before, during and after surgical interventions as well as for examination and treatment.  Part 143302F0 (US)  Part 143302B0 (OUS)

## Reason for recall

Plastic socket of the IEC 60320-1 socket  pulled out of the metal cage and electronic parts exposed; where the socket was pulled out and main cable is still connected to the main socket (power source), there is a risk that a user or third person may suffer an electric shock when coming in contact with the exposed electronic components

## Distribution

Worldwide distribution - US Nationwide and the countries of   ARGENTINA, AUSTRALIA, BAHRAIN, BOLIVIA, BRAZIL,   BULGARIA, CANADA, CHILE, CHINA, COLOMBIA, COSTA RICA, CROATIA, CZECH REPUBLIC, FINLAND, FRANCE  GERMANY, HONG KONG, HUNGARY, INDIA, INDONESIA,   IRAQ, ISRAEL, ITALY, JAPAN, KENYA, KOREA, KUWAIT,   LATVIA, LEBANON, MACAU, MACEDONIA, MALAYSIA, MEXICO, NEW ZEALAND, OMAN, POLAND, QATAR,   ROMANIA, RUSSIAN FEDERATION, RWANDA, SAUDI ARABIA, SERBIA, SINGAPORE, SOUTH AFRICA, SPAIN,   SWEDEN, SWITZERLAND, TUNESIA, TURKEY, UNITED ARAB EMIRATES, UNITED KINGDOM.

## Key facts

- **Recall number:** Z-0133-2021
- **Recalling firm:** Maquet Cardiovascular Us Sales, Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2020-09-24
- **Report date:** 2020-10-28
- **Termination date:** 2023-02-28

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Wayne, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=Z-0133-2021

## Citation

> AI Analytics. FDA recall Z-0133-2021. Retrieved 2026-07-03 from https://api.ai-analytics.org/recall/Z-0133-2021. Source: US FDA. Licensed CC0.

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