Class IITerminated in FDA datasetRecall initiated Jan 11, 2014

Markets of Meijer Pretzel Dinner Roll

Recalling firm: Meijer Distribution, Inc

Why it was recalled

Milk not listed as Allergen. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: May 15, 2014.

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Compare the exact product and package details with the label you have.

ProductMarkets of Meijer Pretzel Dinner Roll, 8 count, 14.0 oz ( 0.87 lb) UPC 0-4125099036-9 Ingredients: Enriched Flour ( Wheat Flour, Malted Barley Flour, niacin, iran, thiamine mononitrate....) water, sugar, canola oil, salt, why (milk) , yeast, wheat starch soy lecithin, wheat gluten Allergens: Contains wheat, soy Meijer Distribution, Inc. Grand Rapids, MI 49544
Package size14.0 oz
UPC041250990369

FDA code information

all products with a sell date through 1/15/2014

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Markets of Meijer Pretzel Dinner Roll, 8 count, 14.0 oz ( 0.87 lb) UPC 0-4125099036-9 Ingredients: Enriched Flour ( Wheat Flour, Malted Barley Flour, niacin, iran, thiamine mononitrate....) water, sugar, canola oil, salt, why (milk) , yeast, wheat starch soy lecithin, wheat gluten Allergens: Contains wheat, soy Meijer Distribution, Inc. Grand Rapids, MI 49544

Extracted codes and context

TypeCode / valueContext
UPC041250990369Markets of Meijer Pretzel Dinner Roll, 8 count, 14.0 oz ( 0.87 lb) UPC 0-4125099036-9 Ingredients: Enriched Flour ( Wheat Flour, Malted Barley Flour, niacin, iran, thiamine mononitrate....) water, sugar,

Original FDA recall reason

Milk not listed as Allergen. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

Recall details

Recall number
F-1646-2014
Event ID
67268
FDA status
Terminated
Initiated
Jan 11, 2014
Reported
Mar 19, 2014
Classified
Mar 11, 2014
Terminated
May 15, 2014
Quantity
Approx 8837 for all products
Location
Grand Rapids, MI, United States
Initiation type
Voluntary: Firm initiated
Notification
E-Mail

Where it was distributed

Meijer stores in Illinois, Indiana, Kentucky, Michigan, and Ohio Food Banks in

FDA source record · F-1646-2014

Data updated September 16, 2026. View official FDA data ↗

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