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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:144544

Dimension Vista Blood Urea Nitrogen (BUN) Flex reagent cartridge The BUN method is an in vitro diagnostic test for the quantitative measurement of urea nitrogen (an end product of nitrogen metabolism) in human serum, plasma, and urine on the Dimension Vista System.

Official recall number

Z-1622-2016

Evidence summary

Product code
CDQ
Recall status
Terminated
Event initiated
February 16, 2016
Root cause
Nonconforming Material/Component
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1622-2016

Field note

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