Heartland Products recalls Roma's Italian Base (120116) due to high azodicarbonamide levels and undeclared allergens. Consumers should check packaging for recall details.
Presence of high levels of Azodicarbonamide (ADA), failure to declare allergens on label, and potential cross-contamination with allergens.
Heartland Products is recalling Roma's Italian Base (120:16) because it contains high levels of azodicarbonamide (ADA) and fails to declare allergens on labels. This poses a risk of allergic reactions for people sensitive to these ingredients.
The product contains high levels of azodicarbonamide (ADA), which can cause allergic reactions in sensitive individuals. It also fails to declare allergens on the label, increasing the risk of cross-contamination with other allergens.
People who purchased Roma's Italian Base (120116) from Heartland Products, Inc. in Des Moines, IA. Those with allergies to ADA or undeclared allergens are most at risk.
Check for the product name 'Roma's Italian Base', batch number 120116, and packaging in 50-lb. poly-lined cardboard boxes. The product was manufactured by Heartland Products, Inc. in Des Moines, IA.
Look for the batch number 120116 on the product label.
The recall does not state that the product is safe to eat. It contains high levels of azodicarbonamide and fails to declare allergens.
Check for the batch number 12016 on the product label and packaging in 50-lb. poly-lined cardboard boxes.
The recall does not specify a remedy, so no action is required beyond checking if you have the product.
We’ve drafted a message you can send Heartland Products to request your refund or repair — edit it as you like.
Subject: Recall F-1077-2016 — Heartland Products Heartland Products Hello, I own a Heartland Products that is covered by recall F-1077-2016 from Heartland Products. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.