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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:186350

Pro Series Fertility Device (SKU 644042788139)

Official recall number

Z-1363-2021

Evidence summary

Product code
MQF
Recall status
Open, Classified
Event initiated
December 23, 2020
Root cause
No Marketing Application
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-1363-2021

Field note

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