Recall Z-1251-2024— Invacare Corporation
Class II · Ongoing
Class II FDA medical device recall by Invacare Corporation, initiated 2024-01-22. FDA's recall record names no specific 510(k) clearance for this event. Product: 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. Reason: Invacare Homecare & G-Series Bed Components identified with a potential weld defect leads to premature weld failures to occur on these components.
- Recalling firm
- Invacare Corporation
- Classification
- Class II
- Status
- Ongoing
- Initiated
- 2024-01-22
- Firm location
- Elyria, OH, United States
Product description
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
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
Data sourced from openFDA. This site is unofficial and independent of the FDA.