LOW RISK
Terminated
F-1903-2013
Benefiber, Fiber plus Calcium Supplement, Wild Berry Chewables 90ct, sugar free, chewable tablets bottle. 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
26,604 units
Product Type
Food
Code Info
Lot Number and Expiration date 10118852 , 6/30/2013; 10123090, 8/31/2013; 10127095, 10/31/2014.
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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