FDAClass IIISeptember 25, 2013

Benefiber recall

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

Why was Benefiber recalled?

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

What should I do if I have this product?

Review the official FDA enforcement record for current instructions.

What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.

Is my product affected?

Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.

Which lot codes, UPCs or models are affected?

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

Product
Benefiber, Fiber plus Calcium Supplement, Wild Berry Chewables 90ct, sugar free, chewable tablets bottle. Novartis Consumer Health, Inc, Parsippany…
Recalling firm
Novartis Consumer Health
Quantity
26,604 units
Distribution
Distribution was made nationwide.
Recall date
September 25, 2013
Classification
Class III
Status
Terminated
Agency
FDA (food)
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