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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:215795

Allura Xper FD20/15 OR Table; Product Code: 722059; Associated 510(k) numbers: K102005, K130842, K130638, K133292, K141979, K161563, K162859, K033737, K041949;

Official recall number

Z-2634-2025

Evidence summary

Product code
OWB
Recall status
Open, Classified
Event initiated
September 03, 2025
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-2634-2025

Field note

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