Medline PAD9130Recalls & reported problems
Medline Industries, Inc. · PAD, GROUNDING, UNIVERS, SOLID, UNCO · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 2
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10193489082487), received between May 22, 2023 and Sep 24, 2026 — classified as 2 injuries, 3 malfunctions.
The most frequently reported specific device problem is “Compatibility Problem” (2 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.
Reports received per month
Most reported problems
Device problems
- Compatibility Problem2
- Adverse Event Without Identified Device or Use Problem1
- Appropriate Device Problem Term/Code Not Available1
- Use of Device Problem1
Patient problems
- Burn(s)2
- No Clinical Signs, Symptoms or Conditions2
- Superficial (First Degree) Burn1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 24, 2026Compatibility Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50884353 ↗MalfunctionSep 11, 2026Compatibility Problem
It was reported that "these grounding pads would not work. They would not connect with their bovie."
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50732912 ↗MalfunctionSep 9, 2026Adverse Event Without Identified Device or Use Problem
Patient problems: Superficial (First Degree) Burn
MAUDE report 50699614 ↗InjuryAug 16, 2023Use of Device Problem; Use of Device Problem
InjuryMay 22, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE CUSTOMER, THE GROUNDING PAD CAUSED "2 MOON SHAPE BURNS ON POSTERIOR THIGH" AFTER "10 MIN" OF APPLICATION.
Patient problems: Burn(s)
MAUDE report 16973989 ↗
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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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