FDA recall record
PureLife Naturals Adult Multi-Plus Multi-Vitamins & Minerals Plus Herbs, 60 Pure Caps HDPE bottle
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, 2017. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
PureLife Naturals Adult Multi-Plus Multi-Vitamins & Minerals Plus Herbs, 60 Pure Caps HDPE bottle
Reason
Labels indicate "no wheat" "no gluten" and the products contain gluten and wheat or a wheat related allergen.
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.
PureLife Naturals Adult Multi-Plus Multi-Vitamins & Minerals Plus Herbs, 60 Pure Caps HDPE bottle
Code information listed by FDA
Product code: 17502, UPC code: 631257175021, Lot 49370, Exp. Date 8/2015 (Mfg date 8/7/2012); Lot 50923, Exp. Date 8/2015 (Mfg date 8/7/2012); Lot 51406, Exp. Date 10/2015 (Mfg. date 10/22/2012); Lot 52401, Exp. Date 10/2015 (Mfg. date 10/22/2012); Lot 57353, Exp. Date 12/2015 (Mfg. date 12/20/2012); Lot 60265, Exp. Date 12/2015 (Mfg. date 12/20/2012)
Distribution and firm information
Recalling firm listed by FDA: ReNew Life Formulas, Inc.
Firm location listed by FDA: Palm Harbor, FL, United States
Distribution reported by FDA: GA, NC, SC, MD, VA, WV, IL, OH, KY, AR, OK, TX, CO, NM, WY, UT, IN, MI, FL, KS, IA, MO, NE, CA, AZ, MN, ND, SD, WI, CT, MA, ME, NH, RI, VT, NJ, AL, LA, MS, TN, NY, DE, PA, NV, AK, ID, MT, OR, WA, Hawaii and Puerto Rico
Product quantity listed by FDA: 60,781 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.