FDA recall record
Glucosamine 750 mg 120 ct, Capsule, Dosage: 12 capsules, 750 mg ea., three times daily with meals
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 27, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Glucosamine 750 mg 120 ct, Capsule, Dosage: 12 capsules, 750 mg ea., three times daily with meals
Reason
TSN Labs is conducting a field action on Glucosamine 750 mg 120 ct due to inadequate allergen labeling.
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.
Glucosamine 750 mg 120 ct, Capsule, Dosage: 12 capsules, 750 mg ea., three times daily with meals
Code information listed by FDA
Lot #s: 4102801, 2071918.2, 2061401, 2032006
Distribution and firm information
Recalling firm listed by FDA: Novacare, LLC
Firm location listed by FDA: Murray, UT, United States
Distribution reported by FDA: Nationwide. No foreign or VA/govt/military consignees.
Product quantity listed by FDA: 961 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.