Amsco 3080-RRecalls & reported problems
Steris Corporation · The 3080-R Remanufactured Table is a general operating table that can handle a variety of surgical specialties including urology, neurology, pediatrics, ENT and endovascular procedures. · Class 1
- 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 00724995155018), received between Apr 22, 2026 and Apr 22, 2026 — 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Unintended Movement1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionApr 22, 2026Unintended Movement
THE USER FACILITY REPORTED THEIR 3080-R SURGICAL TABLE BEGAN TO "LIFT" OFF THE FLOOR DURING A PATIENT PROCEDURE. THE PROCEDURE WAS SUBSEQUENTLY CANCELLED AND RESCHEDULED. NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 24955414 ↗
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.