Operon OT 8301065Recalls & 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
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 07613327169997), received between Jun 7, 2024 and Nov 27, 2024 — classified as 1 injury, 1 malfunction.
The most frequently reported specific device problem is “Unintended Collision” (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 Collision1
- Unintended Movement1
Patient problems
- Bone Fracture(s)1
- Insufficient Information1
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
InjuryNov 27, 2024Unintended Collision; Unintended Collision
IT WAS REPORTED THAT THE TABLE CABLE BASE CAME DOWN ON A SURGEON'S FOOT DURING A CASE. IT WAS STATED THAT THE TABLE LEG SECTION CAME INTO CONTACT WITH INSTRUMENT TABLE JUST BEFORE INCIDENT WHERE TABLE BASE LIFTED UP AND CAME IN CONTACT WITH SURGEON TOE. THIS RESULTED IN A BROKEN TOE WHICH REQUIRED MEDICAL INTERVENTION.
Patient problems: Bone Fracture(s)
MAUDE report 20800692 ↗MalfunctionJun 7, 2024Unintended Movement; Unintended Movement
IT WAS REPORTED THAT THE STAFF LOWERED THEIR TABLE ON A STOOL WHICH LIFTED THE BASE OFF THE GROUND. WHEN THE STOOL GAVE OUT, THE TABLE LANDED ON A STAFF MEMBERS FOOT. THE USER WAS SENT TO GET XRAYS ON THEIR FOOT. COMPLAINANT WAS NOT AWARE OF X-RAY RESULTS OR IF FURTHER TREATMENT OR MEDICAL INTERVENTION WAS REQUIRED.
Patient problems: Insufficient Information
MAUDE report 19492936 ↗
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- ALLEN 107003Hill-Rom, Inc. · Table, operating-room, electrical1 recall9 reports
- Head-Positioning accessories 1739994Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall1 report
- TS 7500 2067886Baxter 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
- 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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