Device evidence
device-recall:cfres:180134
3/8" FloPump, 32mL, (Sterile), REF 6400S, UDI: (01) 081432102013 1, Sterile EO, Rx Only
Evidence summary
- Product code
- KFM
- Recall status
- Terminated
- Event initiated
- June 24, 2019
- Root cause
- Nonconforming Material/Component
- Product
- Z-0318-2021