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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:209693

Flexima Regular Kit Nephrostomy Catheter System Kit, Material Numbers REF M001271860; To provide external drainage of the urinary tract.

Official recall number

Z-3149-2024

Evidence summary

Product code
FFA
Recall status
Open, Classified
Event initiated
July 18, 2024
Root cause
Packaging process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-3149-2024

Field note

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