MAUDE Adverse Event Report: Maquet GmbH MEERA mobile operating table; Table, Operating-Room, Ac-Powered

Model Number	720001B0
Medical Device Problem Code	Use of Device Problem (1670)
Health Effect - Clinical Code	Crushing Injury (1797)
Date of Event	08/19/2026
Type of Reportable Event	Serious Injury
Event or Problem Description
Getinge became aware of an incident involving a mobile operating table.During a surgical procedure, a nurse activated the base lock mechanism.At the time of lock activation, the surgeon's foot was positioned beneath the table base.Engagement of the base lock resulted in a crush injury to the surgeon's foot.Following visualization of the injury, the surgeon experienced a vasovagal syncope episode, including malaise and required immediate medical attention within the healthcare facility.
Additional Manufacturer Narrative
Additional information will be provided following the conclusion of the investigation.The unique identifier (udi) # information is not available since the device was manufactured before 09/24/2022.E1 initial reporter: (b)(6).

• Brand Name: MEERA mobile operating table
• Common Device Name: Table, Operating-Room, Ac-Powered
• Manufacturer (Section D): Maquet GmbH; kehler strasse 31; rastatt ; GM
• Manufacturer (Section G): Maquet GmbH; kehler strasse 31; rastatt ; GM
• Manufacturer Contact: diana gutekunst ; kehler strasse 31; rastatt ; GM
• MDR Report Key: 50771445
• Report Number: 8010652-2026-0000051
• Device Sequence Number: 21261837
• Product Code: FQO
• UDI-Device Identifier: 04046768124332
• UDI-Public: (01)04046768124332
• Combination Product (Y/N): N
• Initial Reporter Country: BR
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,User Facility,Company Representative
• Initial Reporter Occupation: Nurse
• Type of Report: Initial
• Report Date (Section B): 09/15/2026

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: Yes
• Is this a Product Problem Report?: No
• Operator of Device: Health Professional
• Device Model Number: 720001B0
• Was Device Available for Evaluation?: Yes
• Is the Reporter a Health Professional?: Yes
• Type of Report(Section G): Thirty-Day
• Initial Date Received by Manufacturer: 08/20/2026
• Initial Report FDA Received Date: 09/15/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 05/18/2018
• Is the Device Labeled for Single Use? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Required Intervention
• Patient Sex: Unknown