Milk Chocolate Marshmallow Eggs
Chris A Papas & Son Co recalled this product and the FDA reported the enforcement action on 25 March 2015 as Class II. The recall was initiated by the firm. During an FDA Investigation the firm was notified that their labels lack the declaration of soy and Yellow #5 which are known allergens.
The record
Every field below is published by the FDA in the openFDA food enforcement database. Check the FDA notice before acting on any recall: this page is a reading of the public record, not a substitute for it.
- Product
- Milk Chocolate Marshmallow Eggs
- Reason for recall
- During an FDA Investigation the firm was notified that their labels lack the declaration of soy and Yellow #5 which are known allergens.
- Recalling firm
- Chris A Papas & Son Co
- Firm location
- Covington, Kentucky, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-1449-2015
- Quantity
- 7,380 40 count boxes
- Distribution
- 1 Distributer, 33 Retailers
- Initiated
- 22 January 2015
- Reported by FDA
- 25 March 2015
- Terminated
- 21 September 2015
- Firm notified by
- Other
- Product codes
- Marshmallow eggs #15001 through 15112
Reading this record
Five things about this record are not in the record itself, and each one changes how it should be read.
- Class II means the FDA judged a remote probability of serious harm, or a probability of temporary or medically reversible harm. The class is assigned by an agency health hazard evaluation under 21 CFR 7.41, not by the firm.
- The firm started this recall itself. Most FDA food recalls are voluntary, and a recall is a food safety plan working rather than failing. The circumstances in which the agency asks for one instead are set out in 21 CFR 7.45.
- This is one of 13 records covering the same recall event. The FDA opens one enforcement record per product code, so a recall of a product line appears here many times. Counting these records as 13 separate recalls, which almost every published figure does, overstates it by a factor of 13. Every product code in this event is listed together on the record that covers the whole recall, which is the page a search engine is pointed to for all 13 of them.
- The recall ran for 8 months, from 22 January 2015 to termination on 21 September 2015. Termination means the agency judged that all reasonable effort had been made, under 21 CFR 7.55, and it says nothing about whether product remained in circulation.
- The FDA published the enforcement report 2 months after the firm began the recall.
- Recalls of milk or a dairy product run a median of 7 months, so this one was about typical for its category. Dairy recalls split between pathogen contamination in products that skipped or under-ran pasteurisation and undeclared milk in products that should never have contained it, which is the same allergen viewed from two directions.
Filed under milk and dairy, snacks and confectionery and eggs. A product can sit in more than one.
Other milk and dairy recalls
These are the closest records in the corpus: the same kind of food. Unlike the firm’s own records below, they come from different companies, which is what makes them a pattern rather than a history.
Other records from Chris A Papas & Son Co
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 12 other records name this firm.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2015-03-25 | Milk Opera Cream | Chris A Papas & Son Co | During an FDA Investigation the firm was notified that their labels lack the declaration of soy and Yellow #5 which are known allergens. | Class II |
| 2015-03-25 | White Opera Cream | Chris A Papas & Son Co | During an FDA Investigation the firm was notified that their labels lack the declaration of soy and Yellow #5 which are known allergens. | Class II |
| 2015-03-25 | Peanut Butter | Chris A Papas & Son Co | During an FDA Investigation the firm was notified that their labels lack the declaration of soy and Yellow #5 which are known allergens. | Class II |
| 2015-03-25 | Coconut Easter Eggs | Chris A Papas & Son Co | During an FDA Investigation the firm was notified that their labels lack the declaration of soy and Yellow #5 which are known allergens. | Class II |
| 2015-03-25 | Dark Chocolate Marshmallow Eggs | Chris A Papas & Son Co | During an FDA Investigation the firm was notified that their labels lack the declaration of soy and Yellow #5 which are known allergens. | Class II |
| 2015-03-25 | Maple Nut | Chris A Papas & Son Co | During an FDA Investigation the firm was notified that their labels lack the declaration of soy and Yellow #5 which are known allergens. | Class II |
| 2015-03-25 | Cherry Easter Eggs | Chris A Papas & Son Co | During an FDA Investigation the firm was notified that their labels lack the declaration of soy and Yellow #5 which are known allergens. | Class II |
| 2015-03-25 | French Cream | Chris A Papas & Son Co | During an FDA Investigation the firm was notified that their labels lack the declaration of soy and Yellow #5 which are known allergens. | Class II |
| 2015-03-25 | Dark Opera Cream | Chris A Papas & Son Co | During an FDA Investigation the firm was notified that their labels lack the declaration of soy and Yellow #5 which are known allergens. | Class II |
| 2015-03-25 | Vanilla | Chris A Papas & Son Co | During an FDA Investigation the firm was notified that their labels lack the declaration of soy and Yellow #5 which are known allergens. | Class II |
All 13 records for Chris A Papas & Son Co
All 2015 recalls · All FDA food recall data
Behind every recall is a clause somebody has to produce evidence for at their next audit. Krolda maps supplier documents to the clause they satisfy in FSSC 22000, IFS Food and 21 CFR 117, and routes the corrective action when the evidence is missing.
Early accessRecall records come from the openFDA food enforcement API, published by the U.S. Food and Drug Administration in the public domain. Krolda adds the hazard classification and the clause mapping; neither is an FDA determination. Always check the FDA notice before acting on a recall.