Benefiber, Fiber Supplement, Orange Creme Chewables, Sugar Free, 36ct and 100ct chewable tablet…
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 (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; 10125996, 9/30/2014 and 10109551, 3/31/2015.
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Full FDA record and distribution details
Original product description
Benefiber, Fiber Supplement, Orange Creme Chewables, Sugar Free, 36ct and 100ct chewable tablet bottles. 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-1904-2013
- Event ID
- 66013
- FDA status
- Terminated
- Initiated
- Aug 6, 2013
- Reported
- Sep 25, 2013
- Classified
- Sep 19, 2013
- Terminated
- Nov 4, 2014
- Quantity
- 165,480 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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