FDA Food recall F-1903-2013
Benefiber, Fiber plus Calcium Supplement, Wild Berry Chewables 90ct, sugar free, chewable tablets bottle
- FDA Food
- Class III
- terminated
- Published 2013-09-25
On 2013-09-25 the FDA classified a Class III recall of Benefiber, Fiber plus Calcium Supplement, Wild Berry Chewables 90ct, sugar free, chewable tablets bottle by Novartis Consumer Health, citing the lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
Read the official FDA Food notice
| Agency | FDA Food |
|---|---|
| Recall number | F-1903-2013 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-08-06 |
| Published | 2013-09-25 |
| Last updated | 2026-09-13 11:48 UTC |
| Company | Novartis Consumer Health |
| Distribution | US |
Product
Benefiber, Fiber plus Calcium Supplement, Wild Berry Chewables 90ct, sugar free, chewable tablets bottle. Novartis Consumer Health, Inc, Parsippany, NJ.
Reason
The lot number and/or expiration date may be illegible on the outer plastic bottle packaging.
Identifiers
| code_info | Lot Number and Expiration date 10118852 , 6/30/2013; 10123090, 8/31/2013; 10127095, 10/31/2014. |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:48 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1903-2013%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.