Senor Murphy Santa Fe Candymaker Pecan Bueno, 4oz and 1 lb. Handmade with pecans, sugar…
Senor Murphy Candymaker, LLC recalled this product and the FDA reported the enforcement action on 25 December 2013 as Class II. The recall was initiated by the firm. Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile Pistachio Bark, Chocolate Pretzels, Chile Peanuts, Pinon Brittle, Peanut Brittle, and Chile Peanut Brittle due to undeclared 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
- Senor Murphy Santa Fe Candymaker Pecan Bueno, 4oz and 1 lb. Handmade with pecans, sugar, corn syrup, butter, soda, and salt.
- Reason for recall
- Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile Pistachio Bark, Chocolate Pretzels, Chile Peanuts, Pinon Brittle, Peanut Brittle, and Chile Peanut Brittle due to undeclared allergens.
- Recalling firm
- Senor Murphy Candymaker, LLC
- Firm location
- Santa Fe, New Mexico, United States
- Classification
- Class II
- Status
- Terminated
- Recall number
- F-1123-2014
- Quantity
- 116
- Distribution
- Nationwide. No military/govt/VA or foreign consignees.
- Initiated
- 22 November 2013
- Reported by FDA
- 25 December 2013
- Terminated
- 21 May 2014
- Firm notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Product codes
- ALL codes
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 8 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 8 separate recalls, which almost every published figure does, overstates it by a factor of 8. 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 8 of them.
- The recall ran for 6 months, from 22 November 2013 to termination on 21 May 2014. 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 5 weeks 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.
What this recall was for
Undeclared allergens
An undeclared allergen recall means a food contained one of the major allergens and the label did not say so, either because the wrong label was applied or because an ingredient carried an allergen nobody traced.
A preventive controls plan covers an undeclared allergen under the clauses below. This is where the control belongs, not a finding against any firm named on this page: a recall record states a reason, and most of these recalls were initiated by the firm itself.
- 21 CFR 117.135(c)(2)
- Food allergen controls: the written preventive controls that keep an allergen out of a food it does not belong in, and that get the allergens present onto the label.
- 21 CFR 101.4
- Ingredient declaration: every ingredient listed by its common name, in descending order of predominance, on the label of a packaged food.
- 21 CFR 117 subpart G
- Supply-chain programme: the approval and verification a receiving facility runs on a supplier when the hazard is controlled before the ingredient arrives.
The allergens named in this record: peanuts, tree nuts.
Filed under milk and dairy, nuts and seeds, sauces, dips and condiments, spices and seasonings and beverages and juice. A product can sit in more than one.
Other milk and dairy recalls for the same reason
These are the closest records in the corpus: the same kind of food, recalled for a hazard this record also names. 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 Senor Murphy Candymaker, LLC
The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 7 other records name this firm.
| Reported | Product | Firm | Reason | Class |
|---|---|---|---|---|
| 2013-12-25 | Senor Murphy Santa Fe Candymaker Peanut Brittle , 4 oz and 1 lb. | Senor Murphy Candymaker, LLC | Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile Pistachio Bark, Chocolate Pretzels, Chile Peanuts, Pinon Brittle, Peanut Brittle, and Chile Peanut Brittle due to undeclared allergens. | Class II |
| 2013-12-25 | Senor Murphy Santa Fe Candymaker Pinon Brittle , 4 oz and 1 lb. Handmade with pinones (pine nuts), sugar, corn syrup, butter, soda, and salt. | Senor Murphy Candymaker, LLC | Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile Pistachio Bark, Chocolate Pretzels, Chile Peanuts, Pinon Brittle, Peanut Brittle, and Chile Peanut Brittle due to undeclared allergens. | Class II |
| 2013-12-25 | Senor Murphy Santa Fe Candymaker Cashew Crunch , 4oz and 1 lb. Handmade with cashews, sugar, corn syrup, butter, soda, and salt. | Senor Murphy Candymaker, LLC | Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile Pistachio Bark, Chocolate Pretzels, Chile Peanuts, Pinon Brittle, Peanut Brittle, and Chile Peanut Brittle due to undeclared allergens. | Class II |
| 2013-12-25 | Senor Murphy Santa Fe Candymaker Chile Pistachio Bark , 2.5 oz and 1 lb. Handmade with dark chocolate (sugar, chocolate liquor processed with alkali, cocoa butter, milk fat, soy lecithin - an emulsifier, natural flavors), pistachios, chile, salt. | Senor Murphy Candymaker, LLC | Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile Pistachio Bark, Chocolate Pretzels, Chile Peanuts, Pinon Brittle, Peanut Brittle, and Chile Peanut Brittle due to undeclared allergens. | Class II |
| 2013-12-25 | Senor Murphy Santa Fe Candymaker Chocolate Pretzels 3 oz. | Senor Murphy Candymaker, LLC | Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile Pistachio Bark, Chocolate Pretzels, Chile Peanuts, Pinon Brittle, Peanut Brittle, and Chile Peanut Brittle due to undeclared allergens. | Class II |
| 2013-12-25 | Senor Murphy Santa Fe Candymaker Chili Peanut Brittle , 4 oz and 1 lb. Handmade with sugar, corn syrup, peanuts, butter, soda, chile, and salt. | Senor Murphy Candymaker, LLC | Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile Pistachio Bark, Chocolate Pretzels, Chile Peanuts, Pinon Brittle, Peanut Brittle, and Chile Peanut Brittle due to undeclared allergens. | Class II |
| 2013-12-25 | Senor Murphy Santa Fe Candymaker Chile Peanuts, 4 and 9 oz. Handmade with peanuts, sugar, corn syrup, brown sugar, butter, baking soda, Shimayo red chile, and salt. | Senor Murphy Candymaker, LLC | Senor Murphy Candymaker is recalling Pecan Bueno, Cashew Crunch, Chile Pistachio Bark, Chocolate Pretzels, Chile Peanuts, Pinon Brittle, Peanut Brittle, and Chile Peanut Brittle due to undeclared allergens. | Class II |
All 8 records for Senor Murphy Candymaker, LLC
All 2013 recalls · All FDA food recall data
21 CFR 117.135(c)(2) is the clause behind this recall, and it is one 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.