FDA recall record
Benefiber Non-Thickening Powder, Sugar Free, packaged in the following configurations: (1) 2.8-oz. (20 servings) bottles, UPC 300670044206; (2) 4.6-oz. (32 servings) bott...
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 November 26, 2014. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
8-oz. 6-oz. 4-oz. 6-oz. 3-oz. 7-oz. 6-lb. 3-oz. 12-oz. 45-oz. 12-oz. 19-oz. 12-oz. stick packs, UPC 300670030346. , Parsippany, NJ 07054-0622. Made in France.
Reason
The products are being recalled due to the receipt of a relatively high number of consumer complaints.
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.
8-oz. 6-oz. 4-oz. 6-oz. 3-oz. 7-oz. 6-lb. 3-oz. 12-oz. 45-oz. 12-oz. 19-oz. 12-oz. stick packs, UPC 300670030346. , Parsippany, NJ 07054-0622. Made in France.
Code information listed by FDA
8-oz. 6-oz. 4-oz. 6-oz. 3-oz. 7-oz. 6-oz. 2-oz. 3-oz. 12-oz. 45-oz. (28-ct. 19-oz. (28+6 stick pack) boxes: 10107198, 10116607, 10116608, 10122652, and 10122934.
Distribution and firm information
Recalling firm listed by FDA: Novartis Consumer Health
Firm location listed by FDA: Lincoln, NE, United States
Distribution reported by FDA: Product was distributed nationwide and included military distribution. Foreign distribution was made to Panama and Belize.
Product quantity listed by FDA: 19,900,520 consumer 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.