Operon OT 8302065Recalls & reported problems
Berchtold Holding GmbH · Berchtold Surgical Table, D 830 · 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
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327170061), received between Sep 17, 2025 and Aug 18, 2026 — classified as 2 malfunctions.
The most frequently reported specific device problem is “Unintended Movement” (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
- Unintended Movement1
- Unintended System Motion1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 18, 2026Unintended Movement
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50310944 ↗MalfunctionSep 17, 2025Unintended System Motion; Unintended System Motion
IT WAS REPORTED THAT WHEN PUTTING THE TABLE IN REVERSE TREND AND THE TABLE CAME OFF THE GROUND. THEY HAD TO HIT TABLE UP AND IT CAME CRASHING DOWN. THEY WERE DOING A LAP CHOLE AND PATIENT WAS SUPINE IN NORMAL ORIENTATION. THERE WERE INCISIONS MADE, BUT NO HARM WAS DONE. THERE WERE NO REPORTED INJURIES OR ADVERSE CONSEQUENCES.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 23080083 ↗
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- TS 7500 4091000Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall0 reports
- ALLEN 107003Hill-Rom, Inc. · Table, operating-room, electrical1 recall0 reports
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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