Operon OT 1702175Recalls & 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
- 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 07613327169935), received between Jun 30, 2026 and Jun 30, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Positioning 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
- Positioning Problem1
- Unintended Movement1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionJun 30, 2026Positioning Problem; Unintended Movement
IT WAS REPORTED THAT AS CLOSURE STARTED THE BED CONTINUED TO TILT WHICH CAUSED THE PATIENT TO SLIDE REGARDLESS OF SAFETY BELT. THE BED AT THE MOMENT WAS NOT FUNCTIONAL AND DID NOT WANT TO RESPOND TO THE REMOTE COMMANDS TO RETURN TO ORIGINAL FLAT POSITION. THE PATIENT'S CLOSURE OF SKIN ON PORT INCISIONS WAS NOT FULLY CLOSED. THERE WERE NO REPORTED INJURIES OR MEDICAL INTERVENTION.
Patient problems: Insufficient Information
MAUDE report 25668247 ↗
Other TABLE, OPERATING-ROOM, ELECTRICAL devices
- NA 72203299Smith & Nephew, Inc. · TABLE, OPERATING-ROOM, ELECTRICAL298 reports
- 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.
How reports and recalls are matched · Editorial policy · Report an error on this page