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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:115438

Quidel, Sofia Influenza A + B FIA, Kit #20218 (25-Test Kit), in vitro diagnostic.

Official recall number

Z-0819-2013

Evidence summary

Product code
GNX
Recall status
Terminated
Event initiated
December 03, 2012
Root cause
Nonconforming Material/Component
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0819-2013