Kendall SCD 295250 (UDI 10192253023015)Recalls & reported problems
Cardinal Health 200, LLC · Kendall SCD 700 Sequential Compression System · Class 2
- 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 10192253023015), received between Feb 25, 2025 and Feb 25, 2025 — classified as 1 injury.
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
- Adverse Event Without Identified Device or Use 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 25, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem
CUSTOMER REPORTS: WE RECENTLY HAD AN INCIDENT WHERE IT WAS REPORTED BY THE PATIENT THAT THE DEVICE WASN¿T WORKING AND DID NOT INFLATE. THE PATIENT ENDED UP WITH A PULMONARY EMBOLISM (P.E.) UNFORTUNATELY. THE DEVICE'S SERIAL NUMBER WASN¿T TAKEN AS IT WASN¿T REPORTED AT THE TIME OF THE EVENT.
Patient problems: Pulmonary Embolism
MAUDE report 21463710 ↗
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Sources: FDA GUDID, MAUDE and Medical Device Recalls via openFDA. openFDA data is not validated for clinical or regulatory use.