FDA recall record
CALCI-MAX Dietary Supplement, 60 capsules, Manufactured for: DOMEL
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 August 25, 2020. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
CALCI-MAX Dietary Supplement, 60 capsules, Manufactured for: DOMEL
Reason
FDA sample analysis of Calci-Max lot 31453 showed the product zinc content to be 0.0% of label claim.
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.
CALCI-MAX Dietary Supplement, 60 capsules, Manufactured for: DOMEL
Code information listed by FDA
LOT 31453 MFG 06 2019 EXP 06 2022
Distribution and firm information
Recalling firm listed by FDA: Alfa Vitamins Laboratories, Inc.
Firm location listed by FDA: Miami, FL, United States
Distribution reported by FDA: Domestic distribution only.
Product quantity listed by FDA: 1877 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.