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NA Table Pad (REF BF115)Recalls & reported problems

Steris Corporation · The 4-inch TLT Foot Section is used with 3085 Surgical Table. · Class 1

Adverse event reports
6
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 6 adverse event reports that list this exact device (DI 00724995163877), received between Nov 18, 2025 and Feb 5, 2026 — classified as 6 malfunctions.

The most frequently reported specific device problem is “Use of Device Problem” (4 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: 0 reportsAug 2025: 0 reportsSep 2025: 0 reportsOct 2025: 0 reportsNov 2025: 1 reportsDec 2025: 2 reportsJan 2026: 2 reportsFeb 2026: 1 reportsMar 2026: 0 reportsApr 2026: 0 reportsMay 2026: 0 reportsJun 2026: 0 reportsJul 2026: 0 reportsAug 2026: 0 reportsSep 2026: 0 reportsOct 2026: 0 reports2024202520262
Last 36 months. The most recent month may be incomplete.

Most reported problems

Device problems

  • Use of Device Problem4
  • Material Separation1

Patient problems

  • No Clinical Signs, Symptoms or Conditions6

Recent adverse event reports

The 6 most recent of 6 reports, in the reporter's own words as published by the FDA.

  • MalfunctionFeb 5, 2026Use of Device Problem

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

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24273403 ↗
  • MalfunctionJan 15, 2026Use of Device Problem

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

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 24079491 ↗
  • MalfunctionJan 6, 2026

    MATTRESS SEAMS COMING APART.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23973556 ↗
  • MalfunctionDec 18, 2025Use of Device Problem; Use of Device Problem

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

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23843250 ↗
  • MalfunctionDec 18, 2025Use of Device Problem; Use of Device Problem

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

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23842957 ↗
  • MalfunctionNov 18, 2025Material Separation

    SEAMS COMING APART.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 23582428 ↗

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.