NA X-Ray Table TopRecalls & reported problems
Steris Corporation · The Digital X-Ray Top Set is used with the STERIS 4085, 5085 and 5085 SRT General Surgical Tables. · 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 10724995157668), received between May 7, 2026 and May 7, 2026 — classified as 1 malfunction.
The most frequently reported specific device problem is “Manufacturing, Packaging or Shipping 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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Manufacturing, Packaging or Shipping Problem1
Patient problems
- Abrasion1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionMay 7, 2026Manufacturing, Packaging or Shipping Problem
THE USER FACILITY REPORTED THAT THEIR DIGITAL X-RAY TOP SET ARRIVED DENTED/DAMAGED AND WHILE THEIR BIOMED TECHNICIAN WAS HANDLING THE DEVICE HE CUT HIS FINGER. THE USER FACILITY DECLINED TO PROVIDE INFORMATION ABOUT IF THE BIOMED TECHNICIAN SOUGHT OR RECEIVED MEDICAL TREATMENT.
Patient problems: Abrasion
MAUDE report 25116011 ↗
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- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- HarmonyAIR A-Series Suspension SystemSteris Corporation · TABLE, OPERATING-ROOM, AC-POWERED2 recalls0 reports
- MEERA mobile operating table 720001B2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED1 recall19 reports
- MAGNUS operating table system 118001B2MAQUET GmbH · TABLE, OPERATING-ROOM, AC-POWERED1 recall17 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.