FDA Food Recalls

Recalls / Class III

Class IIIF-1903-2013

Product

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

Type
Food
Affected lot / code info
Lot Number and Expiration date 10118852 , 6/30/2013; 10123090, 8/31/2013; 10127095, 10/31/2014.
Quantity
26,604 units

Why it was recalled

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

Recalling firm

Firm
Novartis Consumer Health
Notification channel
Letter
Type
Voluntary: Firm initiated
Address
10401 Hwy 6, N/A, Lincoln, Nebraska 68517-9626

Distribution

Distribution pattern
Distribution was made nationwide.

Timeline

Recall initiated
2013-08-06
FDA classified
2013-09-19
Posted by FDA
2013-09-25
Terminated
2014-11-04
Status
Terminated

Source: openFDA Food Enforcement endpoint. Recall record F-1903-2013. The FDA issues recall classifications as health-hazard assessments, not legal findings.

Class III food recall: Benefiber, Fiber plus Calcium Supplement, Wild Berry Chewables 90ct, sugar free, chewable tablets bo… · FDA Food Recalls