Kendall SCD 295257Recalls & reported problems
Cardinal Health 200, LLC · Kendall SCD 700 Sequential Compression System · Class 2
- Adverse event reports
- 5
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 5 adverse event reports that list this exact device (DI 10884521129603), received between Aug 1, 2017 and Jul 25, 2025 — classified as 1 injury, 4 malfunctions.
The most frequently reported specific device problem is “Split” (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. How this data works · Data updated Oct 13, 2026.
Reports received per month
Most reported problems
Device problems
- Split2
- Adverse Event Without Identified Device or Use Problem1
- Arcing1
- Cut In Material1
- Sparking1
Patient problems
- No Patient Involvement2
- Hematoma1
- No Clinical Signs, Symptoms or Conditions1
- No Information1
Recent adverse event reports
The 5 most recent of 5 reports, in the reporter's own words as published by the FDA.
InjuryJul 25, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
CUSTOMER REPORTS: A HEMATOMA WAS DISCOVERED DURING THE USE OF SCD700, AND AN INCISION WAS REQUIRED FOR RETRIEVAL. I HAVE BEEN USING IT SINCE (B)(6) AND NOTICED THAT A HEMATOMA HAD FORMED ON THE MORNING OF (B)(6) 2025. THE PATIENT HAD EDEMA EVEN BEFORE USING THE SCD700 SYSTEM. IT IS UNKNOWN HOW MUCH EDEMA IT WAS. CURRENTLY, THE TREATMENT IS OVER AND THE PATIENT'S CONDITION IS STABLE, AND SCD IS NOT BEING USED. IT SEEMS THAT THE ALARM DOES NOT GO OFF DURING USE, BUT I ASKED FOR AN INVESTIGATION OF THE MAIN UNIT AND CONSUMABLES TO SEE IF THERE IS A POSSIBILITY THAT THE PRESSURE HAS TEMPORARILY INCREASED. THE USAGE PERIOD WAS 9 DAYS.
Patient problems: Hematoma
MAUDE report 22615550 ↗MalfunctionApr 5, 2021Arcing; Sparking; Arcing; Sparking
THE CUSTOMER REPORTED THAT DURING INSPECTION, WHEN THE POWER CORD WAS PLUGGED IN, SPARKS FLEW FROM THE OUTLET AND THE 3-PIN PART OF THE POWER CORD WAS BURNT. THE DEVICE STARTED UP BUT IT WAS UNABLE TO CHECK THE INSIDE OF IT. THE POWER CORD WAS TORN. THERE WAS A COATING DETACHMENT, BUT NO EXPOSED INTERNAL COPPER WIRE AND METAL CONDUCTOR WIRE. NO ACCESSORIES WERE AFFECTED.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11616196 ↗MalfunctionMay 16, 2018Cut In Material; Cut In Material
THE CUSTOMER REPORTS THE COVER OF POWER CORD WAS DAMAGED. AS A RESULT OF INSPECTION IN OUR LOCAL SERVICE CENTER, COPPER WIRES WERE EXPOSED.
Patient problems: No Patient Involvement
MAUDE report 7520039 ↗MalfunctionDec 8, 2017Split; Split
THE CUSTOMER REPORTS THE PUMP HAS A DAMAGED POWER CORD THAT HAS EXPOSED COPPER WIRE.
Patient problems: No Patient Involvement
MAUDE report 7099122 ↗MalfunctionAug 1, 2017Split; Split
CUSTOMER STATES THAT THE POWER CABLE IS DAMAGED AND COPPER WIRE IS EXPOSED.
Patient problems: No Information
MAUDE report 6757525 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.