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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:196626

X-Guide X-Mark Probe Tool -used for registering edentulous patients to the software or performing XMark registration. Catalog Number:P010673

Official recall number

Z-0222-2023

Evidence summary

Product code
QRY
Recall status
Open, Classified
Event initiated
September 28, 2022
Root cause
Process control
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0222-2023