NA 72200481Recalls & reported problems
Smith & Nephew, Inc. · T-MAX, JAPANESE/ESCHMANN · Class 1
- Adverse event reports
- 2
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 2 adverse event reports that list this exact device (DI 00885554011999), received between Dec 5, 2023 and Jul 28, 2025 — classified as 2 malfunctions.
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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Positioning Problem1
- Unintended Movement1
Patient problems
- No Clinical Signs, Symptoms or Conditions2
Recent adverse event reports
The 2 most recent of 2 reports, in the reporter's own words as published by the FDA.
MalfunctionJul 28, 2025Positioning Problem; Positioning Problem
IT WAS REPORTED THAT, DURING AN ARTHROSCOPIC PROCEDURE, THE T-MAX COULD NOT FIX THE PATIENT'S HEAD, IT WAS POINTED OUT THAT THE BALL AND SOCKET OF THE HEAD REST LOST THE FIXATION. THE PROCEDURE WAS CANCELLED. THE PATIENT WAS ALREADY UNDER ANESTHESIA WHEN THE PROCEDURE WAS CANCELLED. NO FURTHER COMPLICATIONS WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22635975 ↗MalfunctionDec 5, 2023Unintended Movement; Unintended Movement
IT WAS REPORTED THAT DURING A PROCEDURE, THE BACKREST OF THE T-MAX CHAIR SUDDENLY FELL BACKWARDS APPROXIMATELY 45 DEGREES. THE PROCEDURE WAS COMPLETED USING THE SAME DEVICE. THERE WAS NO SURGICAL DELAY AND NO FURTHER COMPLICATIONS WERE REPORTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 18267495 ↗
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- NA 210080Mako Surgical Corp. · Operating Room Accessories Table Tray74 reports
- ALLEN 104002Hill-Rom, Inc. · Operating Room Accessories Table Tray1 recall8 reports
- N/A 7210569Smith & Nephew, Inc. · Accessories, operating-room, table (kit)57 reports
- ALLEN 107004Hill-Rom, Inc. · Operating Room Accessories Table Tray1 recall5 reports
- ALLEN 108001Hill-Rom, Inc. · Operating Room Accessories Table Tray1 recall3 reports
- NA 7210551Smith & Nephew, Inc. · Accessories, operating-room, table (kit)41 reports
- MAYFIELD® A1018Integra Lifesciences Corporation · Operating Room Accessories Table Tray36 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.