Invacare Homecare Series Bed and Invacare G-Series Beds Containing Component Model Numbers: (1) G50 (2) G53 (3) G54 (4)
FDA device recall Z-1251-2024 · posted 2024-03-04 · Open, Classified
Recall details
- Recalling firm
- Invacare Corporation
- 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
- Action taken
- 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
- Status
- Open, Classified
- Product code
- LLI
- Quantity affected
- 8,117 units
- Distribution
- US Nationwide distribution.
- Date initiated
- 2024-01-22
- Date posted
- 2024-03-04
- Location
- Elyria, OH
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