LOW RISK
Terminated
F-1904-2013
Benefiber, Fiber Supplement, Orange Creme Chewables, Sugar Free, 36ct and 100ct chewable tablet 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
165,480 units
Product Type
Food
Code Info
Lot Number and Expiration date (36ct bottle): 10117915, 5/31/2014; 10118335, 7/31/2014; 10120615, 9/30/2014; 10110703A 3/31/2014. (100ct bottle): 10110706, 2/28/2014; 10112140, 2/28/2014; 10113261, 5/31/2014; 10116530, 5/31/2014; 10120059, 7/31/2014; 10120616, 8/31/2014;
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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