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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:197060

VITEK 2 REAGENT GN TEST KIT VTK2 20 CARDS, CATALOG 21341

Official recall number

Z-0787-2023

Evidence summary

Product code
LQM
Recall status
Open, Classified
Event initiated
November 09, 2022
Root cause
Storage
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0787-2023