Mexicantown Wholesale MUFFINS PLAIN recall — FDA F-1699-2012
The firm recalled 26 products for undeclared allergens. This product was recalled due to undeclared milk (nonfat milk), soy (soybean oil and soy flour), and wheat (flour).
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19,449 detailed records are currently available in this category.
The firm recalled 26 products for undeclared allergens. This product was recalled due to undeclared milk (nonfat milk), soy (soybean oil and soy flour), and wheat (flour).
Pomegranate juice contains levels of lead above allowable limits.
The product did not meet the temperature requirements during the manufacturing process.
Based on information received from Kerry Food Ingredients and Flav ours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its…
Based on information received from Kerry Food Ingredients and Flav ours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its…
CJ Foods is recalling CJ Het Oyster (CJ Frozen Oyster) becauase it has been prepared, packed, or held under insanitary conditions whereby it may have become contaminated with filth, or…
Use of Red #5 in Salted Pollock Roe and undeclared Red #5, Yellow #5 and Red #40 in Salted Pollock Roe.
Based on information received from Kerry Food Ingredients and Flavours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its…
Product may contain undeclared milk.
Product may contain undeclared milk.
Inspectional evidence and sample analyses as well as reports of food borne illness outbreaks due to norovirus have led FDA to believe that Korean molluscan shellfish and products containing…
Based on information received from Kerry Food Ingredients and Flav ours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its…
Based on information received from Kerry Food Ingredients and Flav ours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its…
Nishimoto is recalling all Shirakiku Brand Oyster Breaded received from Korea because they have been prepared, packed, or held under insanitary conditions whereby they may have become…
Based on information received from Kerry Food Ingredients and Flav ours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its…
Based on information received from Kerry Food Ingredients and Flav ours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its…
Queso flavored Pringles, 40 gram and 139 gram sizes, sent to distribution centers in Mexico and Grenada are being recalled because the flavoring ingredient ( under a separate recall) may be…
Inspectional evidence and sample analyses as well as reports of food borne illness outbreaks due to norovirus have led FDA to believe that Korean molluscan shellfish and products containing…
Based on information received from Kerry Food Ingredients and Flav ours, Bay Valley Foods is voluntarily recalling approximately 74,000 cases of boxed pasta mix products manufactured by its…
Rong Cheng Trading is recalling all Korean imported frozen shellfish because the product has been prepared, packed, or held under insanitary conditions whereby it may have become…
Khee Trading is recalling Frozen Half Shell Oysters from Korea because the product has been prepared, packed, or held under insanitary conditions whereby it may have become contaminated…
The Broaster Company, LLC is recalling three lots of Broaster Fish Coating 96627 because they contain an undeclared color additive, Yellow Dye No. 6.
Product may contain undeclared milk and almond.
Two ingredients used in production of certain Pasta Roni products, were recalled by the supplier due to potential metal fragment contamination associated with the lactic acid used in…
FDA enforcement reports are classified by potential health hazard. Class I is the most serious classification, while Class II and Class III generally indicate lower levels of risk. The classification shown here comes from the official FDA record.
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This database is designed for discovery and reference. It can help you locate a relevant recall record, identify the recalling firm or NHTSA campaign, compare dates and classifications, and follow the official source. It is not a substitute for a VIN-specific NHTSA check, a manufacturer notice, medical advice or instructions issued by the recalling company.