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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:162625

AUTO REF/KERATOMETER ARK-1s

Official recall number

Z-1348-2018

Evidence summary

Product code
HKO
Recall status
Terminated
Event initiated
December 20, 2017
Root cause
Equipment maintenance
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1348-2018

Field note

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