Quickie IRISRecalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00016958046861), received between Sep 30, 2022 and Sep 30, 2022 — classified as 1 injury.

The most frequently reported specific device problem is “Retraction 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. 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.

• InjurySep 30, 2022Retraction Problem; Unintended Movement; Retraction Problem; Unintended Movement

  DEALER REPORTS THAT WHEN THE WHEELCHAIR IS IN RECLINE, THE RIGHT PISTON IS NOT HOLDING IN PLACE, CAUSING THE CHAIR TO GRADUALLY LEAN MORE TO THE RIGHT SIDE. THE CAREGIVER REPORTS THAT THE LEAN AND THE CONTINUED USE OF THE WHEELCHAIR DESPITE THE LEAN HAS ALLEGEDLY LED TO THE RIDER EXPERIENCING A STIFF NECK, CONTRACTURES AND AN EXCESSIVE BUILDUP OF SECRETIONS THAT REPORTEDLY REQUIRES MORE BREATHING TREATMENTS/ASSISTANCE COUGHING. ALSO, THE CAREGIVER REPORTS NEW PRESSURE POINTS ARE ALLEGEDLY FORMING. NO PRESSURE SORES ARE REPORTED.

  Patient problems: Cramp(s) /Muscle Spasm(s); Neck Stiffness; Unspecified Respiratory Problem

  MAUDE report 15514599 ↗