FDA recall record
Arthri-D 120ct
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 June 19, 2018. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Arthri-D 120ct
Reason
Product may be contaminated with 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.
Arthri-D 120ct
Code information listed by FDA
Lot# 1701-092
Distribution and firm information
Recalling firm listed by FDA: ABH Nature's Products, Inc.
Firm location listed by FDA: Edgewood, NY, United States
Distribution reported by FDA: Direct to MA and PA
Product quantity listed by FDA: 10,100 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.