FDA recall record
Thyroid Resilience 120 count bottle packaged in an amber plastic bottle with black cap
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 7, 2018. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Thyroid Resilience 120 count bottle packaged in an amber plastic bottle with black cap
Reason
Recalled dietary supplements may contain undeclared milk.
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.
Thyroid Resilience 120 count bottle packaged in an amber plastic bottle with black cap
Code information listed by FDA
Lot # 2114667 and 2061167
Distribution and firm information
Recalling firm listed by FDA: Progressive Laboratories, Inc
Firm location listed by FDA: Irving, TX, United States
Distribution reported by FDA: Nationwide through the United States
Product quantity listed by FDA: 469 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.