LOW RISK
Terminated
F-1905-2013
Benefiber, Fiber Supplement, 72ct and 114 caplet bottles. Novartis Consumer Health, Inc, Parsippany, NJ.
Recalled by Novartis Consumer Health
Classification
Class III — Products that are unlikely to cause any adverse health reaction, but that violate FDA labeling or manufacturing laws.
Reason for Recall
The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
Product Details
Product Quantity
504,456 units
Product Type
Food
Code Info
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;
Voluntary/Mandated
Voluntary: Firm initiated
Distribution & Geography
Distribution Pattern
Distribution was made nationwide.
Company Location
Lincoln, NE, 68517-9626
Timeline
Report Date
09/25/2013
Recall Initiated
08/06/2013
Classification Date
09/19/2013
Termination Date
11/04/2014
Source: U.S. Food & Drug Administration (FDA) — FDA Recalls
Last updated: August 29, 2026
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