FDA recall record
Saba Shark Cartilage Complex Dietary Supplement, 500 mg, 60 Capsules, Distributed by Saba 711 NE 39th Street, Oklahoma City, OK 73105
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 February 9, 2016. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Saba Shark Cartilage Complex Dietary Supplement, 500 mg, 60 Capsules, Distributed by Saba 711 NE 39th Street, Oklahoma City, OK 73105
Reason
The product is being recalled due to the potential presence of Salmonella.
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.
Saba Shark Cartilage Complex Dietary Supplement, 500 mg, 60 Capsules, Distributed by Saba 711 NE 39th Street, Oklahoma City, OK 73105
Code information listed by FDA
Lot number 416349, 08/16
Distribution and firm information
Recalling firm listed by FDA: AMS Health Sciences
Firm location listed by FDA: Oklahoma City, OK, United States
Distribution reported by FDA: Nationwide throughout the US and in Canada
Product quantity listed by FDA: 2,014 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.