Maquet Yuno Mobile Operating Table Recalled for Electric Shock Risk
Maquet is recalling Yuno Mobile Operating Tables because a plastic socket may pull out, exposing electronic parts and creating an electric shock hazard.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product (electric shock) where injury has not yet been reported, which aligns with the High severity criteria in the rubric.
Plain-English summary
Maquet Cardiovascular US Sales, LLC is recalling 62 units of the Yuno Mobile Operating Table in the United States. The recall involves Part 143301F0 with serial numbers 1 through 90. The product is intended to support and position patients before, during, and after surgical interventions, as well as for examination and treatment.
The recall is due to a defect where 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 while the socket is pulled out, there is a risk that a user or third person may suffer an electric shock upon contact with the exposed components.
The affected units were distributed nationwide in the US and in numerous countries worldwide, including Argentina, Australia, Canada, China, France, Germany, India, Japan, and the United Kingdom. The source text does not report any specific illnesses or injuries associated with this defect.
The recalled product
- Product
- 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)
- Manufacturer
- Maquet Cardiovascular Us Sales, Llc
- Category
- Medical Device — Operating Table
- Hazard
- Affected units
- 62
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (1)
- Part 143301F0: SN 1 to SN 90 Part 143301B0: SN 1 to SN 267 (OUS)
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 2 recalled by Maquet Cardiovascular Us Sales, Llc under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
See all 2 products in this recall →Related recalls
Same manufacturer · Maquet Cardiovascular Us Sales, Llc
See all →- HighMaquet Cardiovascular Recalls HLS Set Advanced Due to Sterility Breaches
FDA (Devices) · 2020-12-23
- HighMaquet Cardiovascular Recalls HLS Set Advanced Due to Sterility Breach
FDA (Devices) · 2020-12-23
- HighMaquet BMU 40 Blood Monitoring Units Recalled for Electrical Safety Non-Compliance
FDA (Devices) · 2020-11-18
- HighMaquet Yuno II Mobile Operating Table Recalled for Electric Shock Risk
FDA (Devices) · 2020-10-28
- LowMaquet Rotaflow System Console Instructions for Use Recall
FDA (Devices) · 2020-09-23
Same hazard · electric shock
See all →- High
- Severe
- ModeratePanasonic Electric Toaster Ovens Recalled for Shock and Fire Hazards
CPSC · 2026-07-16
- SevereAltec Recalls 2022-2023 Aerial Work Platforms Due to Missing Check Valve
NHTSA · 2025-12-23
- High