LOW RISK Terminated F-1906-2013

Benefiber, Fiber Supplement, Assorted Fruit, Sugar Free, 100ct chewable tablets. 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

419,040 units

Product Type

Food

Code Info

Lot Number and Expiration date 10110708, 5/12/2011; 10110806, 5/10/2011; 10111858, 6/8/2011; 10112132, 6/17/2011; 10113256, 7/25/2011; 10116303, 9/9/2011; 10116444, 9/8/2011; 10118336, 10/6/2011; 10118337, 10/6/2011; 10119374, 10/31/2011; 10119376, 10/4/2011; 1012

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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