MAUDE Adverse Event Report: MAQUET GMBH CORIN MOBILE OPERATING TABLE; TABLE, OPERATING-ROOM, AC-POWERED

Model Number	770001B2
Medical Device Problem Code	Device Tipped Over (2589)
Health Effect - Clinical Code	Crushing Injury (1797)
Date of Event	04/22/2026
Type of Reportable Event	Serious Injury
Additional Manufacturer Narrative
Additional information will be provided following the conclusion of the investigation.E1 initial reporter: (b)(6).
Event or Problem Description
Getinge became aware of an issue involving one of our tables ¿ 770001b2 corin mobile operating table.While pushing a table to the side of the theatre, the base of the table caught the nurse¿s foot, injuring her big toe.The nurse attended the emergency department, where the toe was cleaned and dressed.She was advised that she is likely to lose the toenail completely, as it was partially torn from the nail bed.No other injuries were reported.We have decided to report the issue due to the serious injury sustained by the user.

• Brand Name: CORIN 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: 25239095
• Report Number: 8010652-2026-0000039
• Device Sequence Number: 16077393
• Product Code: FQO
• UDI-Device Identifier: 04046768145207
• UDI-Public: (01)04046768145207(11)251121
• Combination Product (Y/N): N
• Initial Reporter Country: UK
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: Foreign,Health Professional,User Facility,Company Representative
• Initial Reporter Occupation: Nurse
• Type of Report: Initial
• Report Date (Section B): 05/21/2026

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: 770001B2
• 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: 04/23/2026
• Initial Report FDA Received Date: 05/21/2026
• Was Device Evaluated by Manufacturer? (Y/N): Yes
• Date Device Manufactured: 11/21/2025
• Is the Device Labeled for Single Use? (Y/N): No
• Usage of Device: Reuse
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other
• Patient Sex: Female