FDA recall record
Digest Ultra, dietary supplement, packaged 56 capsules per bottle or distributed in bulk, sold under brand YOR. Product distributed OUTSIDE the US has Spanish label.
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 2, 2015. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Digest Ultra, dietary supplement, packaged 56 capsules per bottle or distributed in bulk, sold under brand YOR. Product distributed OUTSIDE the US has Spanish label.
Reason
Dietary supplement products are recalled because they were made from ingredient that was contaminated with Chloramphenicol.
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.
Digest Ultra, dietary supplement, packaged 56 capsules per bottle or distributed in bulk, sold under brand YOR. Product distributed OUTSIDE the US has Spanish label.
Code information listed by FDA
LOT Numbers: 1207408; MFG -03/12; 1217703; MFG -06/12; 10190112; MFG -01/12; 10190112; MFG -01/12; 10190312; MFG-03/12; 10190313; MFG -03/13; 10191112; MFG -11/12; 20190313; EXP- 2/2015; 20190612; EXP- 06/14; 20191012; EXP -10/14; 1019A0811; EXP- 08/13 ;
Distribution and firm information
Recalling firm listed by FDA: Health Wright Products Inc
Firm location listed by FDA: Clackamas, OR, United States
Distribution reported by FDA: Distributed to California, Florida, Oregon, Utah, and Mexico
Product quantity listed by FDA: 82,906 bottles and 1,552,319 capsules (bulk) in US and 62766 bottles OUTSIDE the US
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.