Severity
Low
FDA Food recall · Reported September 25, 2013
The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
Novartis Consumer Health recalled Benefiber, Fiber Supplement, 72ct and 114 caplet bottles. Novartis Consumer Health, Inc, … - a low-severity action.
Benefiber, Fiber Supplement, 72ct and 114 caplet bottles. Novartis Consumer Health, Inc, … was recalled by Novartis Consumer Health in September 25, 2013. Reason: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.. Check the official notice for the remedy. Verify recall #F-1905-2013 with the FDA Food before acting.
The recall
Novartis Consumer Health issued this low-severity FDA Food recall-The lot number and/or expiration date may be illegible on the outer plastic bottle packaging..
Sourced from official FDA Food enforcement records. Verify recall #F-1905-2013 with the agency before acting. Full product description, hazard, remedy, and related recalls are below.
This FDA Food action (record #F-1905-2013) was formally reported on September 25, 2013, with the manufacturer initiating the action on August 6, 2013. It is classified under Low severity (Class III), 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 504,456 units, a scale large enough to require multi-state distribution tracking.
The documented reason for this recall is: The lot number and/or expiration date may be illegible on the outer plastic bottle packaging. Distribution data in the federal record shows the product reached: Distribution was made nationwide.. 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 - 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.
Where this recall sits in its category - 3,731 children & baby products 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 low severity.
Counts reflect market size and reporting activity, not inherent danger, we do not rank products by risk from raw recall volume.
Severity
Low
Affected scope
504,456 units
Related Recalls
6
0 from same agency
Benefiber, Fiber Supplement, 72ct and 114 caplet bottles. Novartis Consumer Health, Inc, Parsippany, NJ.
The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
| Attribute | Value |
|---|---|
| Agency | U.S. Food and Drug Administration |
| Severity class | Low (Class III) |
| Status | Terminated |
| Recall number | F-1905-2013 |
| Date reported | September 25, 2013 |
| Date initiated | August 6, 2013 |
| Recalling firm | Novartis Consumer Health |
| Firm location | Lincoln, NE |
| Affected scope | 504,456 units |
| Distribution | Distribution was made nationwide. |
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.
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.
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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 September 25, 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.