FDA recall record
ZOE brand Daily 30+ Prebiotic blend; Dietary Supplement; 500g resealable pouch
FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.
FDA listed a termination date of March 3, 2025. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
ZOE brand Daily 30+ Prebiotic blend; Dietary Supplement; 500g resealable pouch
Reason
Product may contain foreign objects: small metal pieces and/or stones
Products involved
Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.
ZOE brand Daily 30+ Prebiotic blend; Dietary Supplement; 500g resealable pouch
Code information listed by FDA
Expiration Date: 10/31/25 batch numbers: 24269, 24287, 24288
Distribution and firm information
Recalling firm listed by FDA: Zoe US, Inc.
Firm location listed by FDA: Canton, MA, United States
Distribution reported by FDA: Arizona, California, Colorado, Connecticut, District of Columbia, Florida, Georgia, Hawaii, Illinois, Kentucky, Maine, Massachusetts, Michigan, Minnesota, New Jersey, New Mexico, New York, North Carolina, Pennsylvania, South Carolina, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin
Product quantity listed by FDA: 142 units
Source
Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.
Official FDA openFDA food enforcement record
Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.