Device evidence

device-recall:cfres:144711

Dimension Assays: Uric Acid (URCA)

Official recall number

Z-1662-2016

Evidence summary

Product code: KNK
Recall status: Terminated
Event initiated: March 17, 2016
Root cause: Device Design
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-1662-2016