Class IIITerminated in FDA datasetAug 6, 2013

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

Recalling firm: Novartis Consumer Health

Why it was recalled

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

Check the codes ↓

The exact product

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

Check the codes

Compare these FDA-provided codes, lot numbers or dates with the product you have.

Match the product, size and code together. A similar name alone does not identify your batch.

Original FDA code information

Lot Number and Expiration date 10118852 , 6/30/2013; 10123090, 8/31/2013; 10127095, 10/31/2014.

Recall details

Recall number
F-1903-2013
Event ID
66013
FDA status
Terminated
Initiated
Aug 6, 2013
Reported
Sep 25, 2013
Classified
Sep 19, 2013
Terminated
Nov 4, 2014
Quantity
26,604 units
Location
Lincoln, NE, United States
Initiation type
Voluntary: Firm initiated
Notification
Letter

Where it was distributed

Distribution was made nationwide.

FDA source record · F-1903-2013

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

A missing code match is not a guarantee of safety. Follow official FDA and manufacturer guidance.