# FDA recall Z-1734-2019

> **Maquet Cardiovascular Us Sales, Llc** · Class II · device recall initiated 2019-05-06.

## Product

GETINGE MEERA MOBILE OPERATING TABLE:  (1) Part 720001B2   (2) Part 720001B0   (3) Part 720001F2   (4) Part 720001F0   (5) Part 710001B2   (6) Part 710001B0   (7) Part 710001F0     Product Usage:  The Meera Mobile Operating Table is designed to support and position the patient immediately before, during and after surgical interventions as well as for examination and treatment.

## Reason for recall

User may suffer an electric shock when coming in contact with the exposed electronic components

## Distribution

Worldwide - US Nationwide Distribution  Foreign:  ALGERIA  ANGOLA  ARGENTINA  AUSTRALIA  AUSTRIA  BAHRAIN  BANGLADESH  BELGIUM  BOLIVIA  BOTSWANA  BOSNIA  AND HERZEGOVINA  BRAZIL  BULGARIA  CANADA  CHILE  CHINA  COLOMBIA  COSTA RICA  CROATIA  CZECH REPUBLIC  DENMARK  ECUADOR  EGYPT  FINLAND  FRANCE  GABON  GERMANY  GREECE  HONG KONG  HONDURAS  HUNGARY  ICELAND  INDIA  IRAN  IRELAND  ISRAEL  ITALY  JAPAN  JORDAN  KUWAIT  LATVIA  LEBANON  LITHUANIA  MACEDONIA  MALAYSIA  MAURITIUS  MEXICO  MOLDAVA  MONTENEGRO  MOROCCO  MYANMAR  NETHERLANDS  NAMIBIA  NORWAY  NEW ZEALAND  PAKISTAN    PARAGUAY  PERU  PHILIPPINES  POLAND  PORTUGAL  ROMANIA  SAUDI ARABIA  SERBIA  SINGAPORE  SLOVAKIA  SLOVENIA  SOUTH AFRICA  SOUTH KOREA  SPAIN  SWEDEN  SWITZERLAND  SYRIA  TAIWAN  TANZANIA  THAILAND  TURKEY  TURKMENISTAN  UKRAINE  UNITED ARAB EMIRATES  URUGUAY  UNITED KINGDOM  VIETNAM

## Key facts

- **Recall number:** Z-1734-2019
- **Recalling firm:** Maquet Cardiovascular Us Sales, Llc
- **Classification:** Class II
- **Product type:** device
- **Status:** Terminated
- **Initiation date:** 2019-05-06
- **Report date:** 2019-06-12
- **Termination date:** 2022-07-06

- **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-1734-2019

## Citation

> AI Analytics. FDA recall Z-1734-2019. Retrieved 2026-06-02 from https://api.ai-analytics.org/recall/Z-1734-2019. Source: US FDA. Licensed CC0.

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