Operon OT 8601165Recalls & reported problems
Berchtold Holding GmbH · Berchtold Surgical Table, D860 · Class 1
All models of Operon (11)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 07613327170177), received between Aug 29, 2024 and Aug 29, 2024 — classified as 1 malfunction.
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
Patient problems
- Bruise/Contusion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionAug 29, 2024Unintended Movement; Unintended Movement
IT WAS REPORTED THAT AFTER INCISIONS AND TROCARS WERE SET WHILE PUTTING THE TABLE INTO REVERSE TRENDELENBURG POSITION THE TABLETOP WAS NOT MOVING INTO POSITION. THE FOOT END OF THE TABLE WAS OFF THE FLOOR ABOUT 6-8". AS IT WAS ATTEMPTED TO LEVEL OUT THE TABLE, THE TABLE QUICKLY RETURNED TO THE FLOOR. THIS CASUED THE NURSE TO LOSE HER BALANCE AND FALL CAUSING THEIR KNEE TO HIT THE FLOOR. THE PATIENT HAD NO INJURIES DURING THIS EVENT AND REQUIRED NO INTERVENTION. THE PROCEDURE RESUMED WITHOUT ANY OTHER INCIDENTS. IT WAS NOTED THAT EQUIPMENT WAS UNDER TABLE¿S LEG SECTION. AFTER THAT EQUIPMENT WAS MOVED, NO FURTHER ISSUES OCCURRED. THE NURSE HAD A BONE BRUISE AND A CONTUSION ON HER KNEE. NO INTERVENTION WAS DONE ON HER, BUT SHE WILL NEED FOLLOW-UP ON HER HEALING. SHE WAS WORKING THE FOLLOWING DAY.
Patient problems: Bruise/Contusion
MAUDE report 20102121 ↗
Other TABLE, OPERATING-ROOM, ELECTRICAL devices
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- TS 7000 1723633Baxter Medical Systems GmbH + Co. KG · TABLE, OPERATING-ROOM, ELECTRICAL1 recall22 reports
- 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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