Check the Batch
Class IITerminated in FDA datasetRecall initiated May 7, 2013

Benefiber Fiber Drink Mix, Kiwi Strawberry, 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, Kiwi Strawberry, Sugar Free, packaged in 5.0-oz. boxes containing 24/0.21-oz. stick packs, UPC 300670106249. Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622. Made in France.
UPC300670106249

FDA code information

10114419, 10115003, 10118673, 10121091, 10121092, 10121093, 10121094, 10123826, 10125460, and 10125461

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Benefiber Fiber Drink Mix, Kiwi Strawberry, Sugar Free, packaged in 5.0-oz. boxes containing 24/0.21-oz. stick packs, UPC 300670106249. Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622. Made in France.

Extracted codes and context

TypeCode / valueContext
UPC300670106249, Sugar Free, packaged in 5.0-oz. boxes containing 24/0.21-oz. stick packs, UPC 300670106249. 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-1962-2013
Event ID
65111
FDA status
Terminated
Initiated
May 7, 2013
Reported
Oct 9, 2013
Classified
Sep 30, 2013
Terminated
Nov 26, 2014
Quantity
152,016/5.0-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-1962-2013

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

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