Benefiber Fruit Chewables (Novartis) – illegible packaging (2013)
Class III: A situation in which use of, or exposure to, a violative product is not likely to cause adverse health consequences
Class III recall indicates unlikely adverse health consequences.
This AI-generated summary is provided for general informational purposes only and is derived from publicly available recall notices. It supplements but does not replace official agency classifications or safety instructions.
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Benefiber, Fiber Supplement, Assorted Fruit, Sugar Free, 100ct chewable tablets. Novartis Consumer Health, Inc, Parsippany, NJ.
Brand
Novartis Consumer Health
Lot Codes / Batch Numbers
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
Products Sold
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;
Novartis Consumer Health is recalling Benefiber, Fiber Supplement, Assorted Fruit, Sugar Free, 100ct chewable tablets. Novartis Consumer H due to The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.. This is a Class I recall, indicating a high risk of serious health consequences. Based on FDA enforcement report.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
Recommended Action
Per FDA guidance
Consumers should stop using the product and contact the recalling firm or return it to the place of purchase.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticePage updated: Jan 6, 2026