Walgreens 369359Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00311917171371), received between Sep 23, 2026 and Sep 23, 2026 — classified as 1 malfunction.

The most frequently reported specific device problem is “Fracture” (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.

• MalfunctionSep 23, 2026Fracture

  It was reported that "it failed this past weekend (Sat May 17). Both legs of the support bar came apart, separating from the screws that connect the support bar to the base assembly."

  Patient problems: No Clinical Signs, Symptoms or Conditions

  MAUDE report 50872069 ↗