Benefiber — Class III food recall F-1906-2013
Terminated recall by Novartis Consumer Health, reported 2013-09-25, distributed nationwide. The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
| Recall number | F-1906-2013 |
|---|---|
| Product type | Food |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Novartis Consumer Health, Lincoln, NE, United States |
| Recall initiated | 2013-08-06 |
| Classified | 2013-09-19 |
| Reported by FDA | 2013-09-25 |
| Terminated | 2014-11-04 |
| Distributed | Nationwide (US) |
| Quantity | 419,040 units |
| Lot numbers | 10110708, 10110806, 10111858, 10112132, 10113256, 10116303, 10116444, 10118336, 10118337, 10119374, 10119376, 10120002, 10120003, 10123092, 10123093, 10125929, 10125995 |
Product
Benefiber, Fiber Supplement, Assorted Fruit, Sugar Free, 100ct chewable tablets. Novartis Consumer Health, Inc, Parsippany, NJ.
Reason for recall
The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/F-1906-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.