INVACARE® BED RAIL 6629Recalls & reported problems

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 00841447102519), received between Aug 12, 2026 and Aug 12, 2026 — 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. What reports can and can't tell you · How this data works · Data updated Oct 16, 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.

• InjuryAug 12, 2026Adverse Event Without Identified Device or Use Problem

  The patient sustained a fracture to her right tibia and fibula when her leg became entrapped within the bed rail structure during an assisted transfer while the rails were in a lowered position. The patient was transferred to the hospital for further evaluation and treatment. Surgical intervention was recommended, but the family refused. The patient received bracing for her leg.

  Patient problems: Limb Fracture

  MAUDE report 50219959 ↗