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