Class IITerminated in FDA datasetRecall initiated May 7, 2013

Benefiber Fiber Supplement Plus Calcium, Orange Natural Flavor, Sugar Free, packaged in…

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.

Check your package

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

ProductBenefiber Fiber Supplement Plus Calcium, Orange Natural Flavor, Sugar Free, packaged in 10.76-oz (48 Servings) bottles, UPC 300670108489. Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622. Made in France.
UPC300670108489

FDA code information

10102129, 10102130, 10102131, 10104656, 10104657, 10104658, 10104659, 10107484, 10114954, 10124211, and 10125514

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 Supplement Plus Calcium, Orange Natural Flavor, Sugar Free, packaged in 10.76-oz (48 Servings) bottles, UPC 300670108489. Distributed by: Novartis Consumer Health, Inc., Parsippany, NJ 07054-0622. Made in France.

Extracted codes and context

TypeCode / valueContext
UPC300670108489ge Natural Flavor, Sugar Free, packaged in 10.76-oz (48 Servings) bottles, UPC 300670108489. 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-1963-2013
Event ID
65111
FDA status
Terminated
Initiated
May 7, 2013
Reported
Oct 9, 2013
Classified
Sep 30, 2013
Terminated
Nov 26, 2014
Quantity
110,664/10.76-oz (48 Servings) bottles
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-1963-2013

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

Follow official FDA and manufacturer guidance.