Curity 9190ARecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10192253047912), received between Mar 26, 2025 and Mar 26, 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.

Most reported problems

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

• InjuryMar 26, 2025Adverse Event Without Identified Device or Use Problem; Adverse Event Without Identified Device or Use Problem

  THE CUSTOMER REPORTED THAT OVER THE LAST 4-5 WEEKS, PATIENTS ARE GETTING REACTIONS SO BAD TO THE PRODUCT, IT LOOKS LIKE BURNS IN A PERFECT OUTLINE OF THE ABDOMINAL PAD SHAPE. THEY ARE HAVING TO TREAT PATIENTS WITH ANTIBIOTICS FOR IT. PER ADDITIONAL INFORMATION RECEIVED, IT WAS A BURN LIKE REACTION IN THE SHAPE OF THE ABDOMINAL PADS. THE PATIENTS WERE PRESCRIBED PREDNISONE. THE ONLY RELIEF THEY GOT WAS WHEN THE ABDOMINAL PADS WERE REMOVED. PHOTOS CANNOT PROVIDE PHOTOS DUE TO PATIENT PRIVACY.

  Patient problems: Skin Inflammation/ Irritation

  MAUDE report 21697320 ↗