Maquet Cardiovascular Us Sales, Llc 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) Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
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)
Brand
Maquet Cardiovascular Us Sales, Llc
Lot Codes / Batch Numbers
Part 143301F0: SN 1 to SN 90 Part 143301B0: SN 1 to SN 267 (OUS)
Products Sold
Part 143301F0: SN 1 to SN 90 Part 143301B0: SN 1 to SN 267 (OUS)
Maquet Cardiovascular Us Sales, Llc is recalling Yuno Mobile Operating Table - Product Usage: Intended for support and position the patient immediate due to 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. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
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
Recommended Action
Per FDA guidance
Getinge issued Urgent Medical Device Recall on September 24, 2020, via FedEx 2 day delivery to US consignees. The letter states reason for recall, health risk and action to take: Per the IFU, section 9.1 (Yuno) and 8.1 (Yuno II), a visual and functional check is required to be performed by a trained person before operation. Follow the instructions in section 4.2.3.1of the Yuno and Yuno II IFU regarding connecting and disconnecting from the mains socket (power source). If the plastic socket of the cold-device plug is pulled out, do not try to put it back into the housing and if there are any exposed electronic components, do not touch them. Disconnect/detach the cable from the main socket, call your in-house technical service and arrange the repair of the table. Per IFU section 9.4 (Yuno) and 8.5 (Yuno II), a defective product may not be used and may not be repaired by yourself. A Getinge Service representative will contact you to schedule the correction. This work will be done at no cost to your facility Please complete and sign the attached URGENT MEDICAL DEVICE RECALL CORRECTION RESPONSE FORM (page 4) to acknowledge that you have received this notification. Return the completed form to Maquet/Getinge by e-mailing a scanned copy to MEERA2019@getinge.com or by faxing the form to 1-973-807-9205
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 10, 2026