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Class III

Novartis Consumer Health

Recall #F-1905-2013 · Initiated 2013-08-06

Product
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.
Quantity affected
504,456 units
Distribution
Distribution was made nationwide.
Lot / 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.
Voluntary / mandated
Voluntary: Firm initiated
Initial notification
Letter
Terminated
2014-11-04

Recalling firm

Novartis Consumer Health
10401 Hwy 6
Lincoln, NE 68517-9626
United States

Recall classification

Unlikely to cause any adverse health consequences.

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