FDA recall record
BTREX PLUS, Dietary Supplement 100 Caplets
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 October 8, 2021. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
BTREX PLUS, Dietary Supplement 100 Caplets
Reason
CGMP Deviations: Presence of damaged tablets
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.
BTREX PLUS, Dietary Supplement 100 Caplets
Code information listed by FDA
Lot # 33491, Exp. 12/22
Distribution and firm information
Recalling firm listed by FDA: Lopez Gonzalez Santana Corporation
Firm location listed by FDA: Rio Piedras, PR, United States
Distribution reported by FDA: Domestic distribution only-PR
Product quantity listed by FDA: 662 bottles.
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.