Medline PAD9135-LPRecalls & reported problems
Medline Industries, Inc. · PAD, GROUNDING, UNIVERSAL, SOLID, 9' · Class 2
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 8
- Deaths reported
- 0
- Injuries reported
- 4
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 8 adverse event reports that list this exact device (DI 10193489082500), received between May 2, 2023 and Sep 11, 2026 — classified as 4 injuries, 4 malfunctions.
The most frequently reported specific device problem is “Insufficient Device Problem Information” (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
- Appropriate Device Problem Term/Code Not Available2
- Insufficient Device Problem Information2
- Adverse Event Without Identified Device or Use Problem1
- Connection Problem1
- Difficult to Open or Remove Packaging Material1
- Loss of or Failure to Bond1
- Use of Device Problem1
Patient problems
- Burn(s)5
- No Clinical Signs, Symptoms or Conditions3
Recent adverse event reports
The 8 most recent of 8 reports, in the reporter's own words as published by the FDA.
MalfunctionSep 11, 2026Loss of or Failure to Bond; Difficult to Open or Remove Packaging Material
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50734318 ↗MalfunctionSep 10, 2026Use of Device Problem
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50722625 ↗MalfunctionSep 9, 2026Adverse Event Without Identified Device or Use Problem
the end of a case a patient had a red burn on their thigh from the bovie pad.
Patient problems: Burn(s)
MAUDE report 50695549 ↗MalfunctionSep 8, 2026Connection Problem
It was reported that Generators not recognizing pads, customer has tried troubleshooting by connecting the same pads to multiple generators.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 50669403 ↗InjuryJul 21, 2025Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE FACILITY ON (B)(6) 2025 THE STAFF MEMBER "APPLIED THE PAD TO PATIENTS' RIGHT THIGH. AFTER SURGERY ABOUT AN INCH SIZE OF SKIN BURN WAS NOTICED WHERE THE GROUNDING PAD WAS APPLIED AND THE ATTENDING BEGAN TO TREAT IT IMMEDIATELY".
Patient problems: Burn(s)
MAUDE report 22554768 ↗InjuryOct 28, 2024Insufficient Device Problem Information; Insufficient Device Problem Information
InjuryJul 13, 2023Appropriate Device Problem Term/Code Not Available; Appropriate Device Problem Term/Code Not Available
ACCORDING TO THE FACILITY ON (B)(6) 2023 DURING AN OR PROCEDURE IN WHICH CAUTERY WAS BEING USED, THE PATIENT EXPERIENCED A BURN ON THEIR "LEFT ANTERIOR THIGH THAT REACHED THE SUBCUTANEOUS TISSUE AND REQUIRED WOUND DEBRIDEMENT AND SUTURES FOR PRIMARY CLOSURE".
Patient problems: Burn(s)
MAUDE report 17321410 ↗InjuryMay 2, 2023Insufficient Device Problem Information; Insufficient Device Problem Information
Other Electrosurgical, cutting & coagulation & accessories devices
- Vasoview Hemopro 2 VH-4000Maquet Cardiovascular LLC · Electrosurgical, Cutting & Coagulation & Accessories6 recalls1 death3,232 reports
- LigaSure LF1937Covidien LP · Electrosurgical, cutting & coagulation & accessories3 deaths2,090 reports
- Olympus WB91051WOLYMPUS Winter & Ibe GmbH · Electrosurgical, Cutting & Coagulation & Accessories1 death1,951 reports
- Valleylab FT10 VLFT10GENCovidien LP · Electrosurgical, cutting & coagulation & accessories1 recall5 deaths1,062 reports
- LigaSure LF1837Covidien LP · ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES1 recall967 reports
- LigaSure LF2019Covidien LP · Electrosurgical, cutting & coagulation & accessories948 reports
- VAPR 225028Depuy Mitek, LLC · ELECTROSURGICAL, CUTTING & COAGULATION & ACCESSORIES895 reports
- LigaSure LF1923Covidien LP · Electrosurgical, cutting & coagulation & accessories855 reports
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.
How reports and recalls are matched · Editorial policy · Report an error on this page