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Novartis Consumer Health

7 recall records in Supplements.

2014

1 record

Class IITerminatedRecall F-1591-2014

Product description

Benefiber fiber supplement stick packs, sugar free and taste free, packaged in the following configurations: (1) Benefiber Fiber Supplement, On-The-Go Stick Packs, Sugar Free, Clear & Taste-Free, packaged in 8.16-oz. boxes containing 68/0.12-oz. stick packs, UPC 300670176686. Distributed by Novartis Consumer Health, Inc., Parsippany, NJ; (2) Benefiber Fiber Supplement, Taste Free, Sugar Free, packaged in 0.36-oz. foil packages containing 3/0.12-oz. stick packs, UPC 300670186036. Distributed by Novartis Consumer Health, Inc., Parsippany, NJ; (3) Benefiber Fiber Supplement, Taste Free, Sugar Free, packaged in 0.36-oz. foil packages containing 3/0.12-oz. stick packs, 8/0.36-oz. foil packages clipped together on a strip, UPC 300679110766. Distributed by Novartis Consumer Health, Inc., Parsippany, NJ;

Reason for recall

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

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Event ID
67373
Code info
68-ct. boxes - 25574002, 25515001, 25515002, and 25574001, all with exp. dates of 02/2014; 3-ct. packages - 26096201, exp. 07/2014; 26096203, exp. 07/2014; 26096202, exp. 07/2014; and 26248201; exp. 05/2014; 8-package clip pack - 26128701, exp. 07/2014, and 26128702, exp. 07/2014.
Product quantity
57,808/68-ct. pkgs., 142,088/3-ct. pkgs., and 11,678/8/3-ct. pkg. clip strips
Distribution pattern
Distribution was nationwide. There was no foreign/military/government distribution.
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
10401 Hwy 6, Lincoln, NE, United States
Recall initiation date
12/18/2013
Center classification date
02/27/2014
Termination date
11/26/2014

2013

6 records

Class IITerminatedRecall F-1959-2013

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.

Reason for recall

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

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Event ID
65111
Code info
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.
Product quantity
226,381 consumer units
Distribution pattern
Product was distributed nationwide and included military distribution. Foreign distribution was made to Panama and Belize.
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
10401 Hwy 6, Lincoln, NE, United States
Recall initiation date
05/07/2013
Center classification date
09/30/2013
Termination date
11/26/2014
Class IITerminatedRecall F-1963-2013

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.

Reason for recall

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

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Event ID
65111
Code info
10102129, 10102130, 10102131, 10104656, 10104657, 10104658, 10104659, 10107484, 10114954, 10124211, and 10125514
Product quantity
110,664/10.76-oz (48 Servings) bottles
Distribution pattern
Product was distributed nationwide and included military distribution. Foreign distribution was made to Panama and Belize.
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
10401 Hwy 6, Lincoln, NE, United States
Recall initiation date
05/07/2013
Center classification date
09/30/2013
Termination date
11/26/2014
Class IIITerminatedRecall F-1903-2013

Product description

Benefiber, Fiber plus Calcium Supplement, Wild Berry Chewables 90ct, sugar free, chewable tablets bottle. Novartis Consumer Health, Inc, Parsippany, NJ.

Reason for recall

The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.

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Event ID
66013
Code info
Lot Number and Expiration date 10118852 , 6/30/2013; 10123090, 8/31/2013; 10127095, 10/31/2014.
Product quantity
26,604 units
Distribution pattern
Distribution was made nationwide.
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
10401 Hwy 6, N/A, Lincoln, NE, United States
Recall initiation date
08/06/2013
Center classification date
09/19/2013
Termination date
11/04/2014
Class IIITerminatedRecall F-1904-2013

Product description

Benefiber, Fiber Supplement, Orange Creme Chewables, Sugar Free, 36ct and 100ct chewable tablet bottles. Novartis Consumer Health, Inc, Parsippany, NJ.

Reason for recall

The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.

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Event ID
66013
Code info
Lot Number and Expiration date (36ct bottle): 10117915, 5/31/2014; 10118335, 7/31/2014; 10120615, 9/30/2014; 10110703A 3/31/2014. (100ct bottle): 10110706, 2/28/2014; 10112140, 2/28/2014; 10113261, 5/31/2014; 10116530, 5/31/2014; 10120059, 7/31/2014; 10120616, 8/31/2014; 10125996, 9/30/2014 and 10109551, 3/31/2015.
Product quantity
165,480 units
Distribution pattern
Distribution was made nationwide.
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
10401 Hwy 6, N/A, Lincoln, NE, United States
Recall initiation date
08/06/2013
Center classification date
09/19/2013
Termination date
11/04/2014
Class IIITerminatedRecall F-1905-2013

Product description

Benefiber, Fiber Supplement, 72ct and 114 caplet bottles. Novartis Consumer Health, Inc, Parsippany, NJ.

Reason for recall

The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.

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Event ID
66013
Code info
Lot Number and Expiration date 72 ct bottle: 10100086, 9/30/2013 114 ct bottle: 10093114, 6/30/2013; 10095522, 7/31/2013; 10095531, 7/31/2013; 10097337, 8/31/2013; 10099444, 9/30/2013; 10099445, 9/30/2013; 10101260, 10/31/2013; 10102755, 11/30/2013; 10104634, 12/31/2013; 10104635, 1/31/2014; 10108857, 1/31/2014; 10112134, 2/28/2014; 10112135, 4/30/2014; 10113255, 5/31/2014; 10116304, 5/31/2014; 10118831, 6/30/2014; 10119626, 6/30/2014; 10120461, 7/31/2014; 10120462, 7/31/2014; 10124311, 9/30/2014; 10128842, 10/31/2014.
Product quantity
504,456 units
Distribution pattern
Distribution was made nationwide.
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
10401 Hwy 6, N/A, Lincoln, NE, United States
Recall initiation date
08/06/2013
Center classification date
09/19/2013
Termination date
11/04/2014
Class IIITerminatedRecall F-1906-2013

Product description

Benefiber, Fiber Supplement, Assorted Fruit, Sugar Free, 100ct chewable tablets. Novartis Consumer Health, Inc, Parsippany, NJ.

Reason for recall

The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.

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Event ID
66013
Code info
Lot Number and Expiration date 10110708, 5/12/2011; 10110806, 5/10/2011; 10111858, 6/8/2011; 10112132, 6/17/2011; 10113256, 7/25/2011; 10116303, 9/9/2011; 10116444, 9/8/2011; 10118336, 10/6/2011; 10118337, 10/6/2011; 10119374, 10/31/2011; 10119376, 10/4/2011; 10120002, 12/6/2011; 10120003, 11/1/2011; 10123092, 12/6/2011; 10123093, 11/18/2011; 10125929, 12/21/2011; 10125995, 12/21/2011;
Product quantity
419,040 units
Distribution pattern
Distribution was made nationwide.
Voluntary / mandated
Voluntary: Firm initiated
Initial firm notification
Letter
Product type
Food
Recalling firm location
10401 Hwy 6, N/A, Lincoln, NE, United States
Recall initiation date
08/06/2013
Center classification date
09/19/2013
Termination date
11/04/2014