Severity
Moderate
ModerateClass IITerminated
FDA Food recall · Reported October 9, 2013
Benefiber Fiber Supplement, Orange Natural Flavor, Non-Thickening Powder, Sugar Free, packaged in 5.7-oz. (35 servings) bottles, UPC 300670068356, 9.4-oz (58 servings) bottles, UPC 300670068585, and 18.7-oz. (115 servings) bottles, UPC 300670068158. Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622, Made in France.
The products are being recalled due to the receipt of a relatively high number of consumer complaints.
Compiled from official public sources by the editorial team.
Verify with FDA Food →
Novartis Consumer Health recalled Benefiber Fiber Supplement, Orange Natural Flavor, Non-Thickening Powder, Sugar Free, pac… - a moderate-severity action.
Benefiber Fiber Supplement, Orange Natural Flavor, Non-Thickening Powder, Sugar Free, pac… was recalled by Novartis Consumer Health in October 9, 2013. Reason: The products are being recalled due to the receipt of a relatively high number of consumer complaints.. Check the official notice for the remedy. Verify recall #F-1959-2013 with the FDA Food before acting.
The recall
Novartis Consumer Health issued this moderate-severity FDA Food recall-The products are being recalled due to the receipt of a relatively high number of consumer complaints..
- Moderate
- severity level
- Class II
- classification
- October 9, 2013
- reported
Sourced from official FDA Food enforcement records. Verify recall #F-1959-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
Recall Insight
This FDA Food action (record #F-1959-2013) was formally reported on October 9, 2013, with the manufacturer initiating the action on May 7, 2013. It is classified under Moderate severity (Class II), with a current status of Terminated. Novartis Consumer Health is listed as the recalling firm, operating out of Lincoln, NE. Federal records list the affected scope as 226,381 consumer units.
The documented reason for this recall is: The products are being recalled due to the receipt of a relatively high number of consumer complaints. Distribution data in the federal record shows the product reached: Product was distributed nationwide and included military distribution. Foreign distribution was made to Panama and Belize.. Distribution scope directly affects the consumer exposure window and determines whether a recall remains regional or escalates into a nationwide advisory.
Within the same product category the archive holds 6 closely related recalls, 6 from FDA Food - clustering in a narrow category often points to a systemic quality-control or supplier issue rather than a one-off defect. Always verify the recall number against the official agency record before acting.
Dietary Supplements recalls over time
Where this recall sits in its category - 2,002 dietary supplements recalls on record
Of 101,704 recalls in the database, 24,878 are high severity, 72,426 moderate, and 4,400 low. This recall is classified moderate severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Affected scope
226,381 consumer units
Related Recalls
6
6 from same agency
Product description
Benefiber Fiber Supplement, Orange Natural Flavor, Non-Thickening Powder, Sugar Free, packaged in 5.7-oz. (35 servings) bottles, UPC 300670068356, 9.4-oz (58 servings) bottles, UPC 300670068585, and 18.7-oz. (115 servings) bottles, UPC 300670068158. Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622, Made in France.
Reason for recall
The products are being recalled due to the receipt of a relatively high number of consumer complaints.
Recall Profile
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Moderate (Class II) |
| Status | Terminated |
| Recall number | F-1959-2013 |
| Date reported | October 9, 2013 |
| Date initiated | May 7, 2013 |
| Recalling firm | Novartis Consumer Health |
| Firm location | Lincoln, NE |
| Affected scope | 226,381 consumer units |
| Distribution | Product was distributed nationwide and included military distribution. Foreign distribution was made to Panama and Belize. |
Profile values are sourced directly from the official FDA Food enforcement record. Source: U.S. Food and Drug Administration.
What to do with this recall
Match your product against the recall record, then act on the agency remedy.
- Check the recall number (F-1959-2013) and product description against the item you own. Search the archive
- Confirm the current status with FDA Food before acting, recall details can be updated.
- Follow the documented remedy (refund, replacement, repair, or disposal) rather than general advice. What to do next
This page summarizes the official FDA Food record for research and awareness; it is not legal, medical, or safety advice. Verify with the issuing agency before acting.
Frequently Asked Questions
What product was recalled? ▼
Benefiber Fiber Supplement, Orange Natural Flavor, Non-Thickening Powder, Sugar Free, packaged in 5.7-oz. (35 servings) bottles, UPC 300670068356, 9.4-oz (58 servings) bottles, UPC 300670068585, and 18.7-oz. (115 servings) bottles, UPC 300670068158. Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622, Made in France.. Recalled by Novartis Consumer Health. Units affected: 226,381 consumer units.
Why was this product recalled? ▼
The products are being recalled due to the receipt of a relatively high number of consumer complaints.
Which agency issued this recall? ▼
This recall was issued by the FDA Food on October 9, 2013. Severity: Moderate. Recall number: F-1959-2013.
Where was the recalled product distributed? ▼
Distribution: Product was distributed nationwide and included military distribution. Foreign distribution was made to Panama and Belize..
How do I check if my product is affected by a recall? ▼
Check the product description and recall number (F-1959-2013) against your product. Visit the official FDA Food website for the most current information. You can also use our Recall Checker tool to search by product name or brand.
What are the health risks of consuming a recalled food product? ▼
Recalled food products may contain contaminants, undeclared allergens, or harmful bacteria such as Salmonella, Listeria, or E. coli. Consuming these products can cause foodborne illness ranging from mild gastrointestinal symptoms to serious conditions requiring hospitalization. If you have consumed a recalled food product and experience symptoms, contact your healthcare provider and report to the FDA via MedWatch.
Nearby Recalls in This Category
Other recalls in the same product category, useful for spotting patterns across the same defect class or manufacturer.
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Compare this recall with Blue Bull Extreme Male Enhancement Supplement, total of 15 … →
Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. This recall: FDA Food, reported October 9, 2013. Severity classes follow each agency's own taxonomy (FDA Class I/II/III; CPSC and NHTSA by hazard type), and related-recall context is computed across the full archive. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.