Kendall SCD UH29525Recalls & reported problems
Cardinal Health, Inc. · KENDALL SCD 700 Sequential Compression System · Class 2
All models of Kendall SCD (12)
Data updated Oct 18, 2026 from official FDA records · Editorial policy
- Adverse event reports
- 1
- Deaths reported
- 0
- Injuries reported
- 1
- Recalls naming it
- 0
Summary
The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10884521155688), received between Feb 11, 2020 and Feb 11, 2020 — classified as 1 injury.
The most frequently reported specific device problem is “Use of Device Problem” (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 18, 2026.
Most reported problems
Device problems
- Use of Device Problem1
Patient problems
- Pulmonary Embolism1
Recent adverse event reports
The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.
InjuryFeb 11, 2020Use of Device Problem; Use of Device Problem
THE CUSTOMER REPORTED THAT THE PATIENT WAS IN THE MEDICAL WARD AND THE DEVICE KEPT ON BEEPING MULTIPLE TIMES . IT WAS NOT WORKING FOR MOST OF THE NIGHT. THE PATIENT¿S TREATMENT WAS CHANGED TO CLEXANE. SHE WAS TRANSFERRED TO (B)(6). EARLY THE NEXT MORNING, THE PATIENT HAD SHARP CHEST PAIN INDICATING A POSSIBLE PULMONARY EMBOLISM. THE PATIENT WAS BLUE LIGHTED TO (B)(6) IN THE EVENING. SHE WAS FOUND TO HAVE A LEFT PULMONARY EMBOLISM EXTENDING FROM THE MAIN PULMONARY ARTERY TO SEGMENTAL AND SUBSEGMENTAL ARTERY.
Patient problems: Pulmonary Embolism
MAUDE report 9695453 ↗
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
- Kendall 84021PCardinal Health 200, LLC · SLEEVE, LIMB, COMPRESSIBLE1 recall0 reports
- Kendall 84021BCardinal 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
- 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 18, 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