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Aloe Cadabra

Live Well Brands, Inc. · Model AP90 · UDI-DI 00826804006952

HGD
1
510(k) clearances
16
Adverse events
2
Recalls
61
Facilities

Recalls

DateFirmReason
2024-04-08MEDLINE INDUSTRIES, LP - NorthfieldMedical convenience kits contain plastic syringes affected by the FDA Safety Alert issued on March 19, 2024. Leaks, breakage, and/ other quality issues have been identified that ma
2012-02-07Carefusion 2200 IncThe povidone-iodine (PVP-I) solution bottles in the trays may have loose caps, allowing leakage and also elevated levels of ethylene oxide (EO) sterilant and/or by-products within

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.