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FDA recall record

Dough base/premix packaged in 30-lb. poly-lined cardboard boxes, manufactured under the following labels: (1) Heartland Products, Inc. Fancy Breads Italian Base, 090108. Ma...

Recall F-1075-2016Class IIITerminatedAugust 27, 2015

FDA classification. FDA Class I, II, and III are not the same as USDA FSIS classifications and are not a cross-agency safety score.

FDA listed a termination date of April 14, 2016. openFDA does not treat this as a live recall-status tracker.

Product described in an FDA recall

Dough base/premix packaged in 30-lb. poly-lined cardboard boxes, manufactured under the following labels: (1) Heartland Products, Inc. Fancy Breads Italian Base, 090108. Manufactured by Heartland Products, Inc., Des Moines, IA; and (2) Northern Lights Pizza, 090108, Manufactured by Heartland Products, Inc., Des Moines, IA.

Reason

Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.

Products involved

Product descriptions are copied from the FDA recall record. They are not a current catalog and are not automatically matched to WhoMadeMyFood product pages.

  • Dough base/premix packaged in 30-lb. poly-lined cardboard boxes, manufactured under the following labels: (1) Heartland Products, Inc. Fancy Breads Italian Base, 090108. Manufactured by Heartland Products, Inc., Des Moines, IA; and (2) Northern Lights Pizza, 090108, Manufactured by Heartland Products, Inc., Des Moines, IA.

Code information listed by FDA

(1) G0601 and (2) G0301

Distribution and firm information

Recalling firm listed by FDA: Heartland Products Inc.

Firm location listed by FDA: Des Moines, IA, United States

Distribution reported by FDA: Product was distributed in IA and IL. No foreign, military, or federal goverment distribution.

Product quantity listed by FDA: (1) 24 - 30 lb. boxes and (2) 24- 30 lb. boxes

Source

Source: U.S. Food and Drug Administration (FDA), openFDA food enforcement reports.

Official FDA openFDA food enforcement record

Identifying an FDA recall record does not imply FDA endorsement of WhoMadeMyFood. Methodology.