Stop using nowMedical device recall · FDA · Published September 24, 2020
Maquet Yuno Mobile Operating Table Recall: Electric Shock Risk from Exposed Wiring
Maquet recalls Yuno Mobile Operating Tables with exposed electrical components that could cause electric shock. Affected units have specific serial numbers; stop using immediately to prevent injury.
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
Take action
Contact the company
📍Recalling firmMaquet Cardiovascular Us Sales, Llc45 Barbour Pond Dr · Wayne, NJ 07470-2094
“Maquet Yuno Mobile Operating Table Recall: Electric Shock Risk from Exposed Wiring.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/64153-maquet-yuno-mobile-operating-table-recall-electric-shock-risk-from. Based on FDA recall #Z-0132-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0132-2021%22&limit=1).
Maquet Cardiovascular Us Sales, Llc recalled the Yuno Mobile Operating Table due to electric shock risks from exposed electronic components. The Food and Drug Administration announced the voluntary Class II recall on September 24, 2020.
How to tell if you have it
Brand: Maquet
Product: Yuno Mobile Operating Table
Part 143301F0 (US), Serial Number 1 to SN 90
Part 143301B0 (OUS), Serial Number 1 to SN 267
The hazard
The plastic socket of the IEC 60320-1 socket may pull out of the metal cage, exposing electronic parts. If the main cable remains connected to the power source, users or third persons risk electric shock upon contact with these exposed components.
Context
GovInfoNow's records show Maquet Cardiovascular Us Sales, Llc has 14 other recalls on record since October 25, 2018. Other recent recalls of similar products include the Maquet HLS Set Advanced 7.0 Recall (November 20, 2020), the Maquet BMU 40 Blood Monitor Recall (September 30, 2020), and the Maquet Rotaflow Console Recall (August 7, 2020).
How to tell if you have this one
Check for Yuno Mobile Operating Tables with serial numbers SN 1 to SN 90 (US) or SN 1 to SN 267 (other countries). The product is intended for surgical patient positioning.
Brand
Maquet
Category
Medical device
FDA recall event · 2 products
All 2 products in this recall
FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.
Classification
Class II
Status
Terminated
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.
Recall number
Product, codes & lots
Quantity
Z-0132-2021
Yuno Mobile Operating Table - Product Usage: Intended for support and position the patient immediately before, during and after surgical interventions as well as for examination and treatment. Part 143301F0 (US) Part 143301B0 (OUS); Part 143301F0: SN 1 to SN 90 Part 143301B0: SN 1 to SN 267 (OUS)
62 units US
Z-0133-2021
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); Part 143302F0-Serial Numbers: SN 1 to SN 13 Part 143302B0-Serial Numbers: SN 1 to SN 62 (OUS)
6 units US
Based on the official FDA remedy
What to do — step by step
Stop Using Immediately
The table poses an electric shock risk if the plastic socket pulls out of the metal cage and electronic parts become exposed.
Where it went and when
Where it was distributed
Distributed nationwide, and outside the U.S.
Nationwide
Not listed
FDA 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,…” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide, and outside the U.S.
Recall timeline
FDA terminated this recall 2.4 years after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #Z-0132-2021 (September 24, 2020) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-0132-2021 to see it in context.
Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.