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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:197246

VENTANA PD-L1 (SP142) VENTANA PD-L1 (SP142) Assay (Class III, US IVD) 07709374001 VENTANA PD-L1 (SP142) Assay (CE IVD Predictive) 08008540001 VENTANA PD-L1 (SP142) IHC Assay (CE IVD Analytical) 07011571001

Official recall number

Z-0907-2023

Evidence summary

Product code
PLS
Recall status
Open, Classified
Event initiated
November 18, 2022
Root cause
Process design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0907-2023