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Recall Observatory FDA recall evidence

Device evidence

device-recall:cfres:215812

Allura Xper FD20 OR Table; Model Numbers: (1) 722015, (2) 722023, (3) 722035; Associated 510(k)s: K102005, K130638, K130842, K133292, K141979, K162859, K161563;

Official recall number

Z-0008-2026

Evidence summary

Product code
OWB
Recall status
Open, Classified
Event initiated
September 03, 2025
Root cause
Device Design
Source snapshot
5482458777762b1480c71ac49b2913b9c7984bb55aac66a4315d018da7cfed2c
Product
Z-0008-2026

Field note

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