The Father's Table Individual packages labeled in part: ***The Bakery baked with recall — FDA F-0939-2013
Incorrectly labeled with a label that does not list strawberries and color additives (FC&C Red 40 and Blue 1).
Track recent U.S. food recall enforcement reports from the FDA. Review recalled products, reasons, classifications, recalling firms, distribution details and official record identifiers when available.
19,449 detailed records are currently available in this category.
Incorrectly labeled with a label that does not list strawberries and color additives (FC&C Red 40 and Blue 1).
The product contains walnuts and it was packaged in the wrong carton. Due to the mis-packaging the ingredient label does not have walnuts listed.
During a visual inspection from Ohio Dept of Agriculture the firm was notified that they did not list milk in their ingredient statement.
Belmont was notified by their customer, Dymatize, that a consumer complained on an allergic reaction after eating the product. The consumer is allergic to peanuts & peanut protein.
Dawn's Foods, inc. is conducting a voluntary recall of certain seafood products packaged in 5# and 10 oz. containers. This is being done with the abundance of cation due to the fact that we…
During a visual inspection from Ohio Dept of Agriculture the firm was notified that they did not list milk in their ingredient statement.
Kinnikinnick Foods, Inc in Edmonton, Alberta Canada indicated that KeHE Distributors in Bloomington, IN had received pie crusts in association with their recall/allergy alert issued…
Dawn's Foods, inc. is conducting a voluntary recall of certain seafood products packaged in 5# and 10 oz. containers. This is being done with the abundance of cation due to the fact that we…
During a visual inspection from Ohio Dept of Agriculture the firm was notified that they did not list milk in their ingredient statement.
During a visual inspection from Ohio Dept of Agriculture the firm was notified that they did not list milk in their ingredient statement.
Undeclared Allergen (Milk). Firm initiated a voluntary recall of their 25 lb. and 50 lb. bags of Spice Cake Mix that had been distributed since August 2012 due to an undeclared allergen,…
Incorrectly labeled with a label that does not list strawberries and color additives (FC&C Red 40 and Blue 1).
Dawn's Foods, inc. is conducting a voluntary recall of certain seafood products packaged in 5# and 10 oz. containers. This is being done with the abundance of cation due to the fact that we…
The product contains Soy and Wheat and is packaged in cartons in which the ingredient statement is missing.
Dawn's Foods, inc. is conducting a voluntary recall of certain seafood products packaged in 5# and 10 oz. containers. This is being done with the abundance of cation due to the fact that we…
Dawn's Foods, inc. is conducting a voluntary recall of certain seafood products packaged in 5# and 10 oz. containers. This is being done with the abundance of cation due to the fact that we…
The firm discovered that the labeling bears an incorrect strength of 9,000 FCC Units per caplet instead of 3,000 FCC units per caplet.
State of CA inspection found four products that do not declare allergy statements which reflect the use of milk, wheat and eggs.
State of CA inspection found four products that do not declare allergy statements which reflect the use of milk, wheat and eggs.
Potential to be contaminated with Listeria Monocytogenes
Potential to be contaminated with Listeria Monocytogenes
State of CA inspection found four products that do not declare allergy statements which reflect the use of milk, wheat and eggs.
Wegmans has recalled 5 oz. and 11 oz. packages of Organic Spinach and Spring Mix Blend because the product may be contaminated with E. coli O157:H7.
The labels on two-liter batches of Regular and Diet Wild Cherry Pepsi were mistakenly swapped during production. This is potential safety issue for individuals who are sensitive to…
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.