FDA WARNING_LETTER - Snyder's Lance Inc. - June 21, 2017

On June 21, 2017, the FDA collected a surveillance sample of Lance Toast Chee Crackers, 1.75oz., which was found to be misbranded under Section 403(a)(1) of the Federal Food, Drug, and Cosmetic Act [21 U.S.C. § 343(a)(1)]. The product label declared 10% of the Daily Value for iron, but FDA analysis revealed the product contained only 51.7% (original) and 57.2% (check) of the declared amount, which is less than 80% as required by 21 CFR 101.9(g)(4)(ii).

Additionally, the information panel labeling did not meet 21 CFR 101.2(e) due to a barcode intervening within the ingredient list. The product label also failed to declare the street address of the firm, a requirement under 21 CFR 101.5(d) unless listed in a current city or telephone directory.

The FDA advised the manufacturer to take prompt action to correct these violations and prevent future occurrences, warning that failure to comply could result in enforcement actions like seizure or injunction. The letter also noted the new nutrition labeling requirements finalized on May 27, 2016, and encouraged early compliance. The firm must respond in writing within fifteen working days,