Operon OT 8302075Recalls & reported problems
Berchtold Holding GmbH · Berchtold Surgical Table, D 830 · Class 1
All models of Operon (11)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327170092), received between Jan 15, 2020 and Jan 15, 2020 — classified as 1 injury.
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 18, 2026.
Most reported problems
Device problems
- Unintended Movement1
Patient problems
- Perforation1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryJan 15, 2020Unintended Movement; Unintended Movement
IT WAS REPORTED THAT "DURING A PROCEDURE YESTERDAY THE TABLE DROPPED QUICKLY FROM A MID-HEIGHT TO IT'S LOWEST HEIGHT. IT HAS BEEN REPORTED THAT THE PATIENT WAS OPEN AND THERE WERE INSTRUMENTS IN THE BELLY AT THE TIME OF THE EVENT. IT WAS REPORTED TO THE COMPLAINANT THAT THE GALL BLADDER RUPTURED AS A RESULT. NO FURTHER INFORMATION IS KNOWN AT THIS TIME."
Patient problems: Perforation
MAUDE report 9591778 ↗
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- TS 7500 4091000Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall0 reports
- TS 7500 1717021Baxter Medical Systems GmbH + Co. KG · 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 18, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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