FDA recall record
Benefiber, Fiber Supplement, 72ct and 114 caplet bottles. Novartis Consumer Health, Inc, Parsippany, NJ.
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 4, 2014. openFDA does not treat this as a live recall-status tracker.
Product described in an FDA recall
Benefiber, Fiber Supplement, 72ct and 114 caplet bottles. Novartis Consumer Health, Inc, Parsippany, NJ.
Reason
The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
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, Fiber Supplement, 72ct and 114 caplet bottles. Novartis Consumer Health, Inc, Parsippany, NJ.
Code information listed by FDA
Lot Number and Expiration date 72 ct bottle: 10100086, 9/30/2013 114 ct bottle: 10093114, 6/30/2013; 10095522, 7/31/2013; 10095531, 7/31/2013; 10097337, 8/31/2013; 10099444, 9/30/2013; 10099445, 9/30/2013; 10101260, 10/31/2013; 10102755, 11/30/2013; 10104634, 12/31/2013; 10104635, 1/31/2014; 10108857, 1/31/2014; 10112134, 2/28/2014; 10112135, 4/30/2014; 10113255, 5/31/2014; 10116304, 5/31/2014; 10118831, 6/30/2014; 10119626, 6/30/2014; 10120461, 7/31/2014; 10120462, 7/31/2014; 10124311, 9/30/2014; 10128842, 10/31/2014.
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: Distribution was made nationwide.
Product quantity listed by FDA: 504,456 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.