Food Recall Check
Class III · Low risk Terminated Initiated Aug 6, 2013 (13 years ago)

Benefiber Fiber Supplement recall

Recalled by Novartis Consumer Health · Lincoln, NE, United States

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

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

Hard or sharp fragments can cut the mouth or throat, break teeth or cause choking. They usually come from equipment wear or packaging on the production line. All foreign material recalls.

What was recalled

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

Quantity: 419,040 units

Food: Dietary supplements

Lot codes, dates and UPCs

A recall covers only these codes. Compare them with the lot number, best-by date or UPC printed on your package.

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;

Where it was sold

Nationwide.

FDA's distribution note: Distribution was made nationwide.

Low risk, but check. Class III means the product is unlikely to make anyone ill but breaks an FDA rule, often a labeling one. If your package matches, the store will normally refund it. FDA lists this recall as terminated: the company has finished removing the product, so it should no longer be on shelves - but it can still be in a freezer or pantry.

Recalling firm
Novartis Consumer Health
Initiated by
Voluntary: Firm initiated
Recall initiated
Aug 6, 2013
In FDA report of
Sep 25, 2013
Terminated
Nov 4, 2014
FDA recall number
F-1906-2013 · event 66013
Official record
FDA enforcement report search

Also recalled with it (4 more products)

FDA files each product of one recall action separately; these share the same FDA event.

Class III · Low risk Terminated Foreign material

Benefiber Fiber Supplement

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

Novartis Consumer Health Nationwide F-1904-2013
Class III · Low risk Terminated Foreign material

Benefiber Fiber Supplement

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

Novartis Consumer Health Nationwide F-1905-2013
Class III · Low risk Terminated Foreign material

Benefibre Orange Creme Chewables

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

Novartis Consumer Health Nationwide F-1907-2013

Other recalls by Novartis Consumer Health

Class II · Moderate risk Terminated Other

Benefiber fiber supplement stick packs

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

Novartis Consumer Health Nationwide F-1591-2014
Class II · Moderate risk Terminated Other

Benefiber Non-Thickening Powder

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

Novartis Consumer Health Nationwide F-1964-2013
Class II · Moderate risk Terminated Other

Benefiber Fiber Supplement Plus Calcium

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

Novartis Consumer Health Nationwide F-1963-2013
Class II · Moderate risk Terminated Other

Benefiber Fiber Drink Mix

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

Novartis Consumer Health Nationwide F-1962-2013