Operon OT 1702075Recalls & reported problems
Berchtold Holding GmbH · Berchtold Surgical Table, D 850 · Class 1
All models of Operon (11)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327169874), received between Apr 18, 2023 and May 23, 2024 — classified as 2 injuries.
The most frequently reported specific device problem is “Battery Problem” (1 report).
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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Battery Problem1
- Power Problem1
- Unintended Movement1
Patient problems
- Insufficient Information1
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryMay 23, 2024Unintended Movement; Unintended Movement
IT WAS REPORTED THAT DURING A SINUS SURGERY WHILE THE PATIENT WAS UNDER ANESTHESIA, THE LEGS GAVE OUT VERY QUICKLY AND THE TABLE WENT TO BOTTOM, HEAD TILTED FORWARD WITH PATIENT ON TABLE. THE PATIENT WAS NOT REPORTED TO BE INJURED AS THE PATIENT WAS CAUGHT/STOPPED FROM FALLING, BUT DUE TO THIS A TOTAL OF 4 STAFF MEMBER WERE HURT (2 OF THEM NOTED AS INJURED) AND AT LEAST 1 X-RAY NEEDED TO BE PERFORMED. THE PROCEDURE WAS CANCELLED.
Patient problems: Insufficient Information
MAUDE report 19388174 ↗InjuryApr 18, 2023Battery Problem; Power Problem; Battery Problem; Power Problem
IT WAS REPORTED THAT THE D850 TABLE STOPPED WORKING IN THE MIDDLE OF A CASE. THE PATIENT WAS OPEN AND THEY HAD TO CLOSE THE PATIENT AND RESCHEDULE THE SURGERY FOR A LATER DATE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 16765894 ↗
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Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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