Benefiber, Fiber Supplement, Assorted Fruit, Sugar Free, 100ct chewable tablets. Novartis…
Recalling firm: Novartis Consumer Health
The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Nov 4, 2014.
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FDA code information
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; 10120002, 12/6/2011; 10120003, 11/1/2011; 10123092, 12/6/2011; 10123093, 11/18/2011; 10125929, 12/21/2011; 10125995, 12/21/2011;
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Full FDA record and distribution details
Original product description
Benefiber, Fiber Supplement, Assorted Fruit, Sugar Free, 100ct chewable tablets. Novartis Consumer Health, Inc, Parsippany, NJ.
Original FDA recall reason
The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
Recall details
- Recall number
- F-1906-2013
- Event ID
- 66013
- FDA status
- Terminated
- Initiated
- Aug 6, 2013
- Reported
- Sep 25, 2013
- Classified
- Sep 19, 2013
- Terminated
- Nov 4, 2014
- Quantity
- 419,040 units
- Location
- Lincoln, NE, United States
- Initiation type
- Voluntary: Firm initiated
- Notification
- Letter
Where it was distributed
Distribution was made nationwide.
Data updated September 16, 2026. View official FDA data ↗
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