Kendall 83022Recalls & reported problems

Summary

The FDA's MAUDE database contains 4 adverse event reports that list this exact device (DI 10885380186462), received between Apr 21, 2026 and Apr 27, 2026 — classified as 4 malfunctions.

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

Recent adverse event reports

The 4 most recent of 4 reports, in the reporter's own words as published by the FDA.

• MalfunctionApr 27, 2026

  PATIENT'S ASSESSMENT IDENTIFIED LARGE AMOUNT OF BRUISING TO BILATERAL LEGS IN OUTLINE OF SCD [SEQUENTIAL COMPRESSION DEVICE] SLEEVES.

  Patient problems: Bruise/Contusion

  MAUDE report 24997927 ↗
• MalfunctionApr 23, 2026

  PATIENT REFUSED TO WEAR SEQUENTIAL COMPRESSION DEVICE (SCD) LEG SLEEVES DUE TO THEM BEING SCRATCHY, HOT/SWEATY AND UNCOMFORTABLE. NURSE REMOVED THE SCD LEG SLEEVES AND EDUCATED PATIENT TO AMBULATE WITH STAFF THROUGHOUT THE DAY FOR BLOOD CLOT PREVENTION.

  Patient problems: Diaphoresis; Discomfort; Hot Flashes/Flushes; Itching Sensation

  MAUDE report 24965341 ↗
• MalfunctionApr 23, 2026

  PATIENT REFUSED TO WEAR SEQUENTIAL COMPRESSION DEVICE (SCD) LEG SLEEVES BECAUSE IT MAKES HIM SWEAT AND CAUSES IRRITATION ON SHINS AND CALVES.

  Patient problems: Diaphoresis; Skin Inflammation/ Irritation

  MAUDE report 24965304 ↗
• MalfunctionApr 21, 2026

  SEQUENTIAL COMPRESSION DEVICE (SCD) LEG SLEEVES CAUSING INCREASED MOISTURE TO PATIENTS BILATERAL LOWER EXTREMITIES. SLEEVES BECOME VERY MOIST AND THEREFORE PATIENT'S SKIN BECOME MORE MOIST, NEEDING TO BE CHANGED DAILY TO PREVENT SKIN BREAKDOWN. MOISTURE ALSO CAUSING FOUL ODOR.

  Patient problems: Skin Disorders; Wound Odor

  MAUDE report 24937782 ↗