NA Table Pad (REF BF752)Recalls & reported problems
Steris Corporation · The Head Section Assembly with Pad, Digital is used with the STERIS 4085 and 5085 General Surgical Tables. · Class 1
Data updated Oct 16, 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 00724995191139), received between Sep 9, 2022 and Sep 9, 2022 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Most reported problems
Device problems
- Use of Device Problem1
Patient problems
- Insufficient Information1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 9, 2022Use of Device Problem; Use of Device Problem
THE USER FACILITY REPORTED THAT AN EMPLOYEE'S FINGERS GOT CAUGHT BETWEEN THE END RAIL AND THE HEADBOARD ON THEIR DUAL ARTICULATING HEADREST ASSEMBLY WHEN SHE WAS RAISING THE HEAD SECTION. THE USER FACILITY DECLINED TO PROVIDE INFORMATION REGARDING IF THE EMPLOYEE SOUGHT OR RECEIVED MEDICAL TREATMENT.
Patient problems: Insufficient Information
MAUDE report 15392650 ↗
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
- 40" Carbon Fiber Extension 4-030-40Skytron LLC · Surgical Table Cushion1 report
- Split Leg Section 4-030-61Skytron LLC · 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 14, 2026 · each report above links to its original FDA record
- Recalls: FDA Medical Device Recalls, file dated Oct 16, 2026
- Page last rebuilt: Oct 16, 2026. Data downloaded through openFDA, which notes it is not validated for clinical or regulatory use.
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