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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:214671

Custom Tubing Kit: REF: K04-00417, K04-00963, K04-01029

Official recall number

Z-2294-2025

Evidence summary

Product code
OJA
Recall status
Open, Classified
Event initiated
June 05, 2025
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2294-2025

Field note

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