Current FDA corpus
Try an official recall number, a recalling firm, or a phrase from the source record.
Device evidence
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
Field note
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