CORIN mobile operating table 770001A2Recalls & reported problems
MAQUET GmbH · Class 1
1 open recall names this device. See the recall details and contact the manufacturer or your healthcare provider.
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 1
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 04046768145184), received between Apr 17, 2025 and Jun 6, 2025 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Positioning Failure” (3 reports).
1 FDA recall record name this device's identifier, 1 still open.
Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. How this data works · Data updated Oct 13, 2026.
Reports received per month
Recalls naming this device
- Jul 14, 2025Open, Classified
Under certain conditions, such as the simultaneous use of the operating table with other medical devices, including high-frequency (HF) surgical equipment, interference may occur that could prevent the device from performing as intended. If the issue occurs, the operating table is unresponsive to command from both the universal remote control and override panel.
Z-2420-2025 · Root cause: Under Investigation by firm · FDA record ↗
Most reported problems
Device problems
- Positioning Failure3
- Failure to Interrogate1
Patient problems
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 6, 2025Positioning Failure; Positioning Failure
GETINGE BECAME AWARE OF AN ISSUE WITH ONE OF OUR MOBILE TABLES - 770001A2 - CORIN W AUTODRIVE, IPC, EU. AS IT WAS STATED, THE OPERATING TABLE STOPPED WORKING AND WAS NOT RESPONDING TO THE IR AND CABLE REMOTE CONTROLS AS WELL AS THE OVERRIDE PANEL AT THE BEGINNING OF THE COLECTOMY SURGERY. THE TABLE ALSO DID NOT WORK WHEN CONNECTED TO THE MAINS. THE PATIENT HAD TO BE MOVED TO ANOTHER OPERATING TABLE, WHICH RESULTED IN PROLONGED ANESTHESIA TIME. THERE WAS NO INJURY REPORTED, HOWEVER, WE DECIDED TO REPORT THE ISSUE BASED ON THE POTENTIAL FOR SERIOUS INJURY IF THE SITUATION, NAMELY THE OPERATING TABLE NOT RESPONDING TO THE REMOTE CONTROL OR OVERRIDE PANEL, LEADING TO THE INABILITY TO POSITION THE TABLE DURING SURGERY, WAS TO REOCCUR.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22157422 ↗MalfunctionMay 23, 2025Positioning Failure; Failure to Interrogate; Positioning Failure; Failure to Interrogate
MANUFACTURER'S REFERENCE NUMBER (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22077628 ↗MalfunctionApr 17, 2025Positioning Failure; Positioning Failure
MANUFACTURER'S REFERENCE NUMBER (B)(4).
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 21856853 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.