Benefiber, Fiber Supplement, 72ct and 114 caplet bottles. Novartis Consumer Health, Inc, Parsippany, NJ.
Recalling firm: Novartis Consumer Health
Why it was recalled
The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
The exact product
Benefiber, Fiber Supplement, 72ct and 114 caplet bottles. Novartis Consumer Health, Inc, Parsippany, NJ.
Check the codes
Compare these FDA-provided codes, lot numbers or dates with the product you have.
Match the product, size and code together. A similar name alone does not identify your batch.
Original FDA code information
Lot Number and Expiration date 72 ct bottle: 10100086, 9/30/2013 114 ct bottle: 10093114, 6/30/2013; 10095522, 7/31/2013; 10095531, 7/31/2013; 10097337, 8/31/2013; 10099444, 9/30/2013; 10099445, 9/30/2013; 10101260, 10/31/2013; 10102755, 11/30/2013; 10104634, 12/31/2013; 10104635, 1/31/2014; 10108857, 1/31/2014; 10112134, 2/28/2014; 10112135, 4/30/2014; 10113255, 5/31/2014; 10116304, 5/31/2014; 10118831, 6/30/2014; 10119626, 6/30/2014; 10120461, 7/31/2014; 10120462, 7/31/2014; 10124311, 9/30/2014; 10128842, 10/31/2014.
Recall details
- Recall number
- F-1905-2013
- Event ID
- 66013
- FDA status
- Terminated
- Initiated
- Aug 6, 2013
- Reported
- Sep 25, 2013
- Classified
- Sep 19, 2013
- Terminated
- Nov 4, 2014
- Quantity
- 504,456 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 ↗
A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.