Device evidence

device-recall:cfres:187860

NeuMoDx Cartridge, For In Vitro Diagnostic Use on the NeuMoDx 288 and NeuMoDx 96 Molecular Systems, Model Number 100100

Official recall number

Z-1978-2021

Evidence summary

Product code: QJR
Recall status: Terminated
Event initiated: May 04, 2021
Root cause: Material/Component Contamination
Source snapshot: 5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product: Z-1978-2021