Kendall SCD 295250 (UDI 10884521129573)Recalls & reported problems
Cardinal Health, Inc. · 700 Sequential Compression System · Class 2
- Adverse event reports
- 13
- Deaths reported
- 0
- Injuries reported
- 0
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 13 adverse event reports that list this exact device (DI 10884521129573), received between Oct 11, 2017 and Nov 22, 2021 — classified as 13 malfunctions.
The most frequently reported specific device problem is “Temperature Problem” (6 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.
Most reported problems
Device problems
- Temperature Problem6
- Power Problem3
- Thermal Decomposition of Device2
- Cut In Material1
- Electrical Power Problem1
Patient problems
- No Consequences Or Impact To Patient7
- No Information3
- No Patient Involvement2
- No Clinical Signs, Symptoms or Conditions1
Recent adverse event reports
The 13 most recent of 13 reports, in the reporter's own words as published by the FDA.
MalfunctionNov 22, 2021Temperature Problem; Temperature Problem
THE CUSTOMER REPORTED THAT THE DEVICE HAD A BURNT/MELTED POWER CORD, ADDITIONAL INFORMATION WAS RECEIVED STATING THAT THERE WERE NO PATIENT HARM.
Patient problems: No Clinical Signs, Symptoms or Conditions
MAUDE report 12855896 ↗MalfunctionOct 19, 2018Thermal Decomposition of Device; Thermal Decomposition of Device
MalfunctionSep 28, 2018Electrical Power Problem; Electrical Power Problem
THE CUSTOMER REPORTS THAT THERE WAS A BOOTING FAILURE WITH AN AUDIBLE ALARM. A COMPONENT ON THE MAINBOARD WAS BURNT.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7920487 ↗MalfunctionSep 26, 2018Thermal Decomposition of Device; Thermal Decomposition of Device
THE CUSTOMER STATES THAT THERE IS THERMAL DAMAGE ON POWER CABLE.
Patient problems: No Information
MAUDE report 7911384 ↗MalfunctionJun 28, 2018Temperature Problem; Temperature Problem
UPON TRIAGE THE SERVICE CENTER FOUND THE PUMP TO HAVE A DAMAGED POWER CORD HAD BURNING.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7646073 ↗MalfunctionJun 22, 2018Power Problem; Power Problem
THE CUSTOMER REPORTS THE POWER CORD WAS DAMAGED (LIVE PINS MISSING).
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7629447 ↗MalfunctionJun 22, 2018Power Problem; Power Problem
UPON TRIAGE, THE FOLLOWING ISSUE WAS FOUND: A DAMAGED POWER CORD WITH BROKEN LIVE PINS.
Patient problems: No Patient Involvement
MAUDE report 7629026 ↗MalfunctionJun 22, 2018Power Problem; Power Problem
THE CUSTOMER STATES A POWER ISSUE. UPON TRIAGE IT WAS NOTED THAT THE LIVE PIN WAS BROKEN OFF THE PLUG.
Patient problems: No Information
MAUDE report 7628996 ↗MalfunctionJun 8, 2018Temperature Problem; Temperature Problem
THE CUSTOMER REPORTS THE PUMP HAS A POWER ISSUE (COMPRESSOR THERMAL DAMAGE).
Patient problems: No Patient Involvement
MAUDE report 7582861 ↗MalfunctionMay 25, 2018Cut In Material; Cut In Material
THE CUSTOMER STATES A DAMAGED POWER CORD. UPON TRIAGE IT WAS NOTED THAT THERE WAS EXPOSED COPPER WIRES.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7544336 ↗MalfunctionMar 23, 2018Temperature Problem; Temperature Problem
UPON TRIAGE THE SERVICE TECH FOUND THE PUMP TO HAVE A DAMAGED COMPRESSOR AND A BURNT TRACK.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7366321 ↗MalfunctionFeb 8, 2018Temperature Problem; Temperature Problem
THE CUSTOMER REPORTS THE PUMP HAS NO POWER. UPON TRIAGE THE SERVICE TECH FOUND THE PUMP TO HAVE A PHYSICALLY BURNT POWER SUPPLY.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 7251338 ↗MalfunctionOct 11, 2017Temperature Problem; Temperature Problem
ACCORDING TO THE REPORTER, THE DEVICE HAD SCORCHED AND MELTED CABLE. NO PATIENT HARM REPORTED.
Patient problems: No Consequences Or Impact To Patient
MAUDE report 6940683 ↗
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- Kendall 84021BCardinal Health 200, LLC · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
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- Kendall 84021PCardinal Health 200, LLC · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
- N/AStryker Sustainability Solutions, Inc. · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
- N/AStryker Sustainability Solutions, Inc. · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.