FDA recall record
Benefiber Healthy Shape Prebiotic Fiber Supplement, 500G UPC 886790018872
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 1, 2021. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Benefiber Healthy Shape Prebiotic Fiber Supplement, 500G UPC 886790018872
Reason
Fiber prebiotic product potentially contaminated with small plastic pieces
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.
Benefiber Healthy Shape Prebiotic Fiber Supplement, 500G UPC 886790018872
Code information listed by FDA
Lot: MP8B (EXP Sep2021)
Distribution and firm information
Recalling firm listed by FDA: Glaxosmithkline Consumer Healthcare Holdings
Firm location listed by FDA: Warren, NJ, United States
Distribution reported by FDA: Distributed to the following US states: AR, CA, FL, HI, ID, IL, LA, MA, ME, MI, MN, MO, NC, NE, NJ, NY, OH, OR, PA, RI, SC, TX, VA, WA, and WI
Product quantity listed by FDA: 29,844 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.