FDA recall record
SP Standard Process, Cataplex ACP (Product #0700 and 0750) , Dietary supplement, 90 & 360 Tablets, Proprietary Blend: Dried buckwheat ( leaf) juice, buckwheat (seed), carrot (...
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 January 13, 2014. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
, UPC 8 12122 01003 0 18.
Reason
Standard Process, Inc. is voluntarily recalling 3 dietary supplements due to potential Salmonella contamination.
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.
, UPC 8 12122 01003 0 18.
Code information listed by FDA
Lot 114, Lot 114, Best Used By dates of 05/13.
Distribution and firm information
Recalling firm listed by FDA: Standard Process, Inc.
Firm location listed by FDA: Palmyra, WI, United States
Distribution reported by FDA: AL, AZ, AR, CA,CO, CT, DE, DC, FL,GA, IL, IN, IA, KS, KY, LA, ME, MD, MA, MI, MN, MS, MO, NE, NV, NY, NH,NM, NY, NC, OH, OK, PA, RI,SC, TN,TX,VT, VA, WA, WV, WI.
Product quantity listed by FDA: 29,044
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.