Skip to content
Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:195034

VITEK 2 / MYLA VITEK 2 Software versions 8.01, 8.02 (veterinary use only), 9.01, 9.02, 9.03 MYLA Software versions V4.8 and V4.9

Official recall number

Z-1640-2022

Evidence summary

Product code
NSX
Recall status
Open, Classified
Event initiated
July 13, 2022
Root cause
Software design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1640-2022