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Class IITerminated in FDA datasetRecall initiated May 7, 2013

Benefiber Fiber Drink Mix, Cherry Pomegranate, Sugar Free, packaged in 5.0-oz. boxes containing…

Recalling firm: Novartis Consumer Health

Why it was recalled

The products are being recalled due to the receipt of a relatively high number of consumer complaints.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Nov 26, 2014.

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Compare the exact product and package details with the label you have.

ProductBenefiber Fiber Drink Mix, Cherry Pomegranate, Sugar Free, packaged in 5.0-oz. boxes containing 24/0.21-oz. stick packs, UPC 300670107246. Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622. Made in France.
UPC300670107246

FDA code information

10116609, 10118436, 10121279, 10121280, 10122653, 10122654, 10125466, and 10128711

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Full FDA record and distribution details

Original product description

Benefiber Fiber Drink Mix, Cherry Pomegranate, Sugar Free, packaged in 5.0-oz. boxes containing 24/0.21-oz. stick packs, UPC 300670107246. Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622. Made in France.

Extracted codes and context

TypeCode / valueContext
UPC300670107246Sugar Free, packaged in 5.0-oz. boxes containing 24/0.21-oz. stick packs, UPC 300670107246. Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622. Made in France.

Original FDA recall reason

The products are being recalled due to the receipt of a relatively high number of consumer complaints.

Recall details

Recall number
F-1961-2013
Event ID
65111
FDA status
Terminated
Initiated
May 7, 2013
Reported
Oct 9, 2013
Classified
Sep 30, 2013
Terminated
Nov 26, 2014
Quantity
162,408/5.0-oz. (24-ct) boxes
Location
Lincoln, NE, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Product was distributed nationwide and included military distribution. Foreign distribution was made to Panama and Belize.

FDA source record · F-1961-2013

Data updated September 16, 2026. View official FDA data ↗

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