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NA Table Pad (REF BF294)Recalls & reported problems

Steris Corporation · The 4-inch TLT Foot Section is used with the STERIS Cmax, 4085, 5085 and 5085 SRT General Surgical Table. · Class 1

Adverse event reports
5
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 00724995163822), received between Jul 24, 2025 and Sep 18, 2025 — classified as 5 malfunctions.

The most frequently reported specific device problem is “Use of Device Problem” (3 reports).

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

Nov 2023: 0 reportsDec 2023: 0 reportsJan 2024: 0 reportsFeb 2024: 0 reportsMar 2024: 0 reportsApr 2024: 0 reportsMay 2024: 0 reportsJun 2024: 0 reportsJul 2024: 0 reportsAug 2024: 0 reportsSep 2024: 0 reportsOct 2024: 0 reportsNov 2024: 0 reportsDec 2024: 0 reportsJan 2025: 0 reportsFeb 2025: 0 reportsMar 2025: 0 reportsApr 2025: 0 reportsMay 2025: 0 reportsJun 2025: 0 reportsJul 2025: 1 reportsAug 2025: 3 reportsSep 2025: 1 reportsOct 2025: 0 reportsNov 2025: 0 reportsDec 2025: 0 reportsJan 2026: 0 reportsFeb 2026: 0 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520263
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Use of Device Problem3
  • Material Separation1
  • Unraveled Material1

Patient problems

  • No Clinical Signs, Symptoms or Conditions5

Recent adverse event reports

The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 18, 2025Use of Device Problem; Use of Device Problem

    THE USER FACILITY REPORTED VIA MEDWATCH (B)(4) THAT THEIR SEAMS ARE COMING APART ON THE SURGICAL TABLE PAD. NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23085975 ↗
  • MalfunctionAug 20, 2025Use of Device Problem; Use of Device Problem

    THE USER FACILITY REPORTED VIA MEDWATCH (B)(4) THAT THEIR "MATTRESS PULLING APART AT SEAMS". NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22853520 ↗
  • MalfunctionAug 20, 2025Material Separation

    SEAMS COMING APART.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22849528 ↗
  • MalfunctionAug 14, 2025Use of Device Problem; Use of Device Problem

    THE USER FACILITY REPORTED VIA MEDWATCH (B)(4) THAT THEIR "MATTRESSES COMING APART AT SEAMS". NO REPORT OF INJURY.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22803644 ↗
  • MalfunctionJul 24, 2025Unraveled Material

    MATTRESS PULLING APART AT SEAMS.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 22585684 ↗

Other SURGICAL TABLE CUSHION devices

All SURGICAL TABLE CUSHION devices →

Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.