Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Open, Classified

Invacare Homecare Series Bed and Invacare G-Series Beds Containing Component Model Numbers: (1) G50 (2) G53 (3) G54 (4) BAR5490IVC (5) BAR5000IVC (6) 5000IVC (7) 5490IVC (8) 5490LOW

FDA Recall Z-1251-2024 · Posted 2024-03-04

Recalling FirmInvacare Corporation
Recall StatusOpen, Classified
Product CodeLLI
Date Initiated2024-01-22
Product Quantity8,117 units

Reason for Recall

Invacare Homecare & G-Series Bed Components identified with a potential weld defect leads to premature weld failures to occur on these components

Firm Action

Invacare issued Urgent Medical Device Correction letter on 12/22/23. Letter states reason for recall, health risk and action to take: 1.Please locate your affected products Please review your records to locate the affected components. Above is a list of model numbers to assist you with this process. 2. Please contact your provider at the number listed below to have the bed component replaced.

Root Cause

Process design

Distribution Pattern

US Nationwide distribution.

Official Source

View FDA Recall →

Source: FDA Enforcement Report / Recall database. Always confirm against the official FDA record.

↑