NA Table Pad (REF BF409)Recalls & reported problems
Steris Corporation · The 4-inch Leg Section Pad, No Cutout is used with leg section on surgical tables. · Class 1
Data updated Oct 13, 2026 from official FDA records · Editorial policy
- 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 00724995163839), received between Jul 3, 2025 and Jul 3, 2025 — classified as 1 malfunction.
The most frequently reported specific device problem is “Use of Device 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
- Use of Device Problem1
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.
MalfunctionJul 3, 2025Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED VIA MEDWATCH (B)(4) THAT THEIR "MATTRESS SEAMS COMING UNDONE". NO REPORT OF INJURY.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 22393768 ↗
Other SURGICAL TABLE CUSHION devices
- NA Table PadSteris Corporation · SURGICAL TABLE CUSHION6 reports
- NA Table PadSteris Corporation · SURGICAL TABLE CUSHION5 reports
- NA Table PadSteris Corporation · SURGICAL TABLE CUSHION4 reports
- NA Table PadSteris Corporation · SURGICAL TABLE CUSHION3 reports
- NA Table PadSteris Corporation · SURGICAL TABLE CUSHION2 reports
- NA Table PadSteris Corporation · SURGICAL TABLE CUSHION2 reports
- Medline PCD082021Medline Industries, Inc. · Surgical table cushion1 report
- NA Table PadSteris Corporation · SURGICAL TABLE CUSHION1 report
Sources and updates
- Device record: FDA GUDID, file dated Oct 13, 2026 · View this device in AccessGUDID ↗
- Adverse event reports: FDA MAUDE, file dated Oct 13, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 13, 2026
- Page last rebuilt: Oct 13, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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