IHOP Pancake Mix Recalled Nationwide for Foreign Material Contamination
Continental Mills is recalling 240 cases of IHOP Pancake Mix (Item #743-0278) nationwide due to the presence of foreign materials. Affected lots are KX2062 and KX2063 with a best-by date of 9/1/2022.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: Foreign materials in food constitute a risk-of-harm product where injury has not yet been reported. The FDA Class II classification with contamination present but no reported illnesses supports a High severity rating per the recall rubric.
Plain-English summary
Continental Mills is voluntarily recalling IHOP Pancake Mix (Item #743-0278) because the product may contain foreign materials. The recall affects 240 cases with lot codes KX2062 and KX2063, with a best-by date of September 1, 2022. The product is a shelf-stable pancake mix sold in 5-pound boxes with UPC 0 41449 47540 0, distributed nationwide.
The U.S. Food and Drug Administration (FDA) has classified this as a Class II recall. Consumers who have purchased the affected product should not use it and should either discard it or return it to the place of purchase.
For additional information or questions, consumers can contact Continental Mills (Corporate Office) at 18100 Andover Park W, Tukwila, WA 98188-4703.
The recalled product
- Product
- Item # 743-0278, IHOP Pancake. Product is shelf stable and packaged in a box. net wt. 5 lbs., UPC 0 41449 47540 0.
- Manufacturer
- Continental Mills (Corporate Office)
- Category
- Food — Baking Mix
- Affected units
- 240
Is your product affected?
Check your packaging against the codes below. If any of them match, the product is part of this recall.
Lot numbers (2)
- Lot code KX2062 and KX2063
- Best by 9/1/2022.
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 9 recalled by Continental Mills (Corporate Office) under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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