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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:191370

KWIK-STIK, Candida parapsilosis derived from ATCC 22019, REF 0726P. Packaged 2 units per pack. IVD controls.

Official recall number

Z-0543-2022

Evidence summary

Product code
JTR
Recall status
Terminated
Event initiated
February 24, 2021
Root cause
Labeling mix-ups
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0543-2022

Field note

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