Device evidence
device-recall:cfres:191587
1. Arterial Line Kit 20ga x 6" 2. Arterial Line Kit /1 20ga x 6"
Evidence summary
- Product code
- GDY
- Recall status
- Open, Classified
- Event initiated
- January 24, 2022
- Root cause
- Mixed-up of materials/components
- Product
- Z-0563-2022