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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:140795

Nipro Safe Touch TULIP Safety Fistula Needle, FT+152530TP, for use as a blood access device for blood purification and for other treatments requiring an extracorporeal circuit of larger volumes of blood.

Official recall number

Z-0161-2016

Evidence summary

Product code
LLB
Recall status
Terminated
Event initiated
August 13, 2015
Root cause
Mixed-up of materials/components
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0161-2016

Field note

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