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Class II: temporary or reversible health riskTerminated

Novartis Consumer Health Benefiber Fiber Supplement Recall

Benefiber Fiber Supplement, Orange Natural Flavor, Non-Thickening Powder, Sugar Free, p…

Novartis Consumer Health · Lincoln, NE

Risk level
Class II
Reported by FDA
Oct 9, 2013
Recall ID
F-1959-2013
Check your lot numberHow we source this data

Summary

Novartis Consumer Health recalled Benefiber Fiber Supplement starting May 7, 2013. The FDA classified it as Class II (temporary or reversible health risk) and published enforcement report F-1959-2013 on Oct 9, 2013. Reason: The products are being recalled due to the receipt of a relatively high number of consumer complaints. Status: Terminated.

Why it was recalled

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

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.

Lot numbers, UPCs & expiration codes

5.7-oz. (35 servings) bottles: 10100230; 9.4-oz. (58 servings) bottles: 10119358, 10121489, 10121490, 24596401, 24596402, 24680101, and 24767601; and 18.7-oz. (115 servings) bottles: 24596701.

Where it was sold

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

What to do if you have this product

  • Compare the brand, size, and lot/UPC codes on your package with the codes above.
  • If it matches, don't eat it. Return it to the store for a refund or throw it away.
  • Wash surfaces and containers that touched the product.
  • If you feel sick after eating it, contact your doctor. In an emergency call 911.

Recall details

Recall number
F-1959-2013
Classification
Class II
Status
Terminated
Recall initiated
May 7, 2013
FDA report date
Oct 9, 2013
Quantity
226,381 consumer units
Recall type
Voluntary: Firm initiated
Recalling firm
Novartis Consumer Health

Original FDA data

Every field from FDA enforcement report F-1959-2013, exactly as published.

Show all FDA fields
City
Lincoln
State
NE
Status
Terminated
Country
United States
Event ID
65111
Address
10401 Hwy 6
Code information
5.7-oz. (35 servings) bottles: 10100230; 9.4-oz. (58 servings) bottles: 10119358, 10121489, 10121490, 24596401, 24596402, 24680101, and 24767601; and 18.7-oz. (115 servings) bottles: 24596701.
Postal code
68517-9626
Report date
Oct 9, 2013
Product type
Food
Recall number
F-1959-2013
Classification
Class II
Recalling firm
Novartis Consumer Health
Product quantity
226,381 consumer units
Termination date
Nov 26, 2014
Reason for recall
The products are being recalled due to the receipt of a relatively high number of consumer complaints.
Voluntary / mandated
Voluntary: Firm initiated
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.
Distribution pattern
Product was distributed nationwide and included military distribution. Foreign distribution was made to Panama and Belize.
Recall initiation date
May 7, 2013
Initial firm notification
Letter
Center classification date
Sep 30, 2013

How we source this data

Source: U.S. Food and Drug Administration enforcement report F-1959-2013, published Oct 9, 2013. View the source record (openFDA) · FDA enforcement reports

Last checked against FDA data: . Content last changed: .

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