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MAUDE Adverse Event Report: STERIS CORPORATION; SURGICAL TABLE CUSHION
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STERIS CORPORATION; SURGICAL TABLE CUSHION
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Model Number
TABLE PAD
Health Effect - Clinical Code
No Clinical Signs, Symptoms or Conditions (4582)
Date of Event
11/27/2025
Type of Reportable Event
Malfunction
Event or Problem Description
Mattress seams coming apart.
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Brand Name
NA
Common Device Name
SURGICAL TABLE CUSHION
Manufacturer
(Section D)
STERIS CORPORATION
2720 gunter park drive east
montgomery AL 36109
MDR Report Key
23973556
Report Number
23973556
Device Sequence Number
9152327
Product Code
LWG
UDI-Device Identifier
00724995163877
UDI-Public
(01)00724995163877(11)240731
Combination Product (Y/N)
N
Initial Reporter State
VA
Number of Events Summarized
1
Summary Report (Y/N)
N
Reporter Type
User Facility
Initial Reporter Occupation
Nurse
Type of Report
Initial
Report Date
(Section B)
12/11/2025
Report Date
(Section F)
12/11/2025
1
Device was Involved in the Event
1
Patient was Involved in the Event
Is this an Adverse Event Report?
No
Is this a Product Problem Report?
Yes
Device Model Number
TABLE PAD
Device Catalogue Number
BF115
Was Device Available for Evaluation?
Yes
Is the Reporter a Health Professional?
Yes
Was the Report Sent to FDA?
Yes
Device Age
17 MO
Event Location
Hospital
Date Report to Manufacturer
01/06/2026
Initial Date Received by Manufacturer
Not provided
Initial Report FDA Received Date
01/06/2026
Is This a Single-Use Device that was
Reprocessed and Reused on a Patient? (Y/N)
No
Usage of Device
Unknown
Patient Sequence Number
1
Patient Sex
Unknown
Date Report Sent to FDA
12/11/2025
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