FDA recall record
Opalescence Treswhite Supreme Peach Patient Kit
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 July 9, 2013. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Opalescence Treswhite Supreme Peach Patient Kit
Reason
Product was packaged into kits labeled as having a shelf life of 2103-05. The correct shelf life is 2013-05.
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.
Opalescence Treswhite Supreme Peach Patient Kit
Code information listed by FDA
Lot B6LZS, Part number 5705
Distribution and firm information
Recalling firm listed by FDA: Ultradent Products, Inc.
Firm location listed by FDA: South Jordan, UT, United States
Distribution reported by FDA: USA: AL, CA, GA, IL, IN, MA, MD, MI, NJ, OK, PA, SC, UT; 12 International distributors: Germany, China, France, Spain
Product quantity listed by FDA: 104 units
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.