Kendall SCD 9525Recalls & reported problems
Cardinal Health, Inc. · Express Sequential Compression System,Vascular Refill Detection · Class 2
All models of Kendall SCD (12)
Data updated Oct 16, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 3
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 3 adverse event reports that list this exact device (DI 10884521081826), received between Apr 6, 2018 and Jan 11, 2021 — classified as 3 malfunctions.
The most frequently reported specific device problem is “Arcing” (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
- Arcing1
- Cut In Material1
- Smoking1
- Sparking1
Patient problems
- No Clinical Signs, Symptoms or Conditions1
- No Consequences Or Impact To Patient1
- No Information1
Recent adverse event reports
The 3 most recent of 3 reports, in the reporter's own words as published by the FDA.
MalfunctionJan 11, 2021Arcing; Arcing
THE CUSTOMER REPORTED THAT THE OT NURSE NOTICED THAT THE POWER CORD IS BURNT BEFORE USING THE DEVICE. THE PHOTO PROVIDED BY THE CUSTOMER INDICATED EVIDENCE OF ARCING ON THE POWER CORD CLOSEST TO WHERE IT PLUGS INTO THE DEVICE.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 11148718 ↗MalfunctionDec 3, 2020Smoking; Sparking; Smoking; Sparking
THE CUSTOMER REPORTED THAT SPARKS WERE SEEN FROM THE POWER CORD WHEN THE DEVICE WAS RUNNING AND BURNING SMELL WAS DETECTED. AFTER REMOVING FROM THE POWER POINT, A VISIBLE BURNT SPOT WAS DISCOVERED ON THE POWER CORD.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 10942004 ↗MalfunctionApr 6, 2018Cut In Material; Cut In Material
VERIFIED COMPLAINT OF "EXPOSED COPPER WIRE". THE POWER CORD WAS EXAMINED AND THE OUTER SHIELDING CONTAINS A CUT MARK AND THE FIBERS ARE SHREDDED.
Patient problems: No Information
MAUDE report 7404690 ↗
Other Sleeve, Limb, Compressible devices
- Kendall 84021Cardinal Health 200, LLC · SLEEVE, LIMB, COMPRESSIBLE2 recalls0 reports
- Kendall SCD 29525Cardinal Health, Inc. · Sleeve, Limb, Compressible56 reports
- RAW MATERIAL 30MDjo, LLC · SLEEVE, LIMB, COMPRESSIBLE52 reports
- N/AStryker Sustainability Solutions, Inc. · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
- N/AStryker Sustainability Solutions, Inc. · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
- Kendall 84021BCardinal Health 200, LLC · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
- Kendall 84021PCardinal Health 200, LLC · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
- AIRCAST 3011-PLDjo, LLC · SLEEVE, LIMB, COMPRESSIBLE1 recall0 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.
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