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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:192791

Inactivated macrolide-resistant Mycoplasma genitalium

Official recall number

Z-0955-2022

Evidence summary

Product code
OHQ
Recall status
Terminated
Event initiated
March 22, 2022
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0955-2022