Class IITerminated · reported 2017-11-29

Dark Chocolate Coconut Almonds, 10 lbs., 15 lbs., 25 lbs.

GKI Foods, LLC recalled this product and the FDA reported the enforcement action on 29 November 2017 as Class II. The recall was initiated by the firm. GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark chocolate products because they may contain an undeclared milk allergen.

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
Dark Chocolate Coconut Almonds, 10 lbs., 15 lbs., 25 lbs.
Reason for recall
GKI Foods of Brighton, Michigan is voluntarily recalling multiple dark chocolate products because they may contain an undeclared milk allergen.
Recalling firm
GKI Foods, LLC
Firm location
Brighton, Michigan, United States
Classification
Class II
Status
Terminated
Recall number
F-0320-2018
Quantity
1399 cases
Distribution
Domestic: MI, IN, IL, FL, TX, CA., NV, OR, NH, NY, NJ, VA, WI, KY, DE, PA, CT, PR, OH, RI, IA,
Initiated
27 October 2017
Reported by FDA
29 November 2017
Terminated
9 July 2018
Firm notified by
Press Release
Product codes
Retail Dark Chocolate Coconut Almonds manufactured between 01/14/16 to 10/24/17; and Bulk Dark Chocolate Coconut Almonds manufactured between 01/14/16 to 09/05/2017; Lots: Lot# 12517 Lot# 30616 Lot# 33816 Lot# 13117 Lot# 16517 Lot# 20517 Lot# 03117 Lot# 10817 Lot# 12517 Lot# 16517 Lot# 22817 Lot# 27517 Lot# 27517 Lot# 04717

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 21 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 21 separate recalls, which almost every published figure does, overstates it by a factor of 21. 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 21 of them.
  • The recall ran for 8 months, from 27 October 2017 to termination on 9 July 2018. 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 distribution pattern names 20 states, and the FDA published the enforcement report 5 weeks after the firm began the recall.
  • Recalls of nuts or seeds run a median of 7 months, so this one was about typical for its category. Nuts and seeds carry both hazards at once: they are a major allergen in their own right, and as a low-moisture food they hold Salmonella for months without supporting its growth, which is why a nut butter recall can trace to a lot pressed a year earlier.

Named in the distribution pattern: Indiana, Illinois, Florida, Texas, California, Nevada, Oregon, New Hampshire, New York, New Jersey, Virginia, Wisconsin, Kentucky, Delaware, Pennsylvania, Connecticut, Puerto Rico, Ohio, Rhode Island, Iowa. Those pages count recalls by where the RECALLING FIRM sits, which is a different question from where this product went.

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: milk.

Filed under nuts and seeds and snacks and confectionery. A product can sit in more than one.

Other nuts and seeds 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.

ReportedProductFirmReasonClass
2026-09-02Glutinous Rice Balls with Black Sesame Filling NET WT. 14.1 OZ (400 g) Product of China UPC: 6908791000053KHONG GUAN (HQ)Undeclared peanuts.Class I
2026-09-02Byron White FORMULAS A-FNG Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404Byron White Formulas, Inc.Label does not declare walnuts in EnglishClass II
2026-09-02BLACK AND WHITE GLUTINOUS RICE BALLS WITH BLACK SESAME FILLING NET WT. 14.1 OZ (400 g) Product of China UPC: 6908791000084KHONG GUAN (HQ)Undeclared peanuts.Class I
2026-09-02Byron White FORMULAS A-P Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404Byron White Formulas, Inc.Label does not declare walnuts in EnglishClass II
2026-09-02Byron White FORMULAS A-L Complex Herbal Supplement 1.0 fl. oz./30 mL May Contain Nuts (Juglans nigra hull) Byron White Formulas Inc. 3315 Chanate Rd. Suite 1C Santa Rosa, CA 95404Byron White Formulas, Inc.Label does not declare walnuts in EnglishClass II
2026-08-19Dark Chocolate Coconut Almond Bites, 3.17oz, Plastic Pouches, 10 Packages per case.Bazzini LLCUndeclared peanutsClass I
2026-07-22Ice Pop, D'Dioses Pistachio, 1 Bar (81.7 g), with UPC 827912008487D'Dioses Fruit Pops, Inc.May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.Class I
2026-07-08FIRST STREET Dark Chocolate Raisins Net Wt. 9 oz. (255g) UPC 797565011830 INGREDIENTS: DARK CHOCOLATE (SUGAR, CHOCOLATE LIQUOR, COCOA BUTTER, MILK FAT, SOY LECITHIN - AN EMULSIFIER, NATURAL VANILLA FLAVOR), RAISINS, TAPIOCA DEXTRIN, CONFECTIONERS GLAZE. CONTAINS: MILK, SOY PACKED IN A FAICLITY THAT HANDLES PEANUTS, TREE NUTS, WHEAT, SOY, EGG, SESAME, AND MILK PRODUCTS.Western Mixers Produce & Nuts, Inc.Undeclared peanuts.Class I

Other records from GKI Foods, LLC

The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 21 other records name this firm.

ReportedProductFirmReasonClass
2017-11-29Dark Chocolate Almond Bark 10 oz.,10 lbs.GKI Foods, LLCGKI Foods of Brighton, Michigan is voluntarily recalling multiple dark chocolate products because they may contain an undeclared milk allergen.Class II
2017-11-29Dark Chocolate Pretzel Nibs, 15 lbs.GKI Foods, LLCGKI Foods of Brighton, Michigan is voluntarily recalling multiple dark chocolate products because they may contain an undeclared milk allergen.Class II
2017-11-29Dark Chocolate Coffee Beans, 10 lbs., 15 lbs., 25 lbs., 12 pch Display, 8/8 oz., 12/10 oz., 12/8 oz.,GKI Foods, LLCGKI Foods of Brighton, Michigan is voluntarily recalling multiple dark chocolate products because they may contain an undeclared milk allergen.Class II
2017-11-29Dark Chocolate Pecans 25 lbs., 15 lbs., 10 lbs.,GKI Foods, LLCGKI Foods of Brighton, Michigan is voluntarily recalling multiple dark chocolate products because they may contain an undeclared milk allergen.Class II
2017-11-29Dark Chocolate Almond, 12/10 oz., 12/18 oz., 18/14 oz., 8/10 oz., 12/8 oz., 8/8 oz., 18 pc.,GKI Foods, LLCGKI Foods of Brighton, Michigan is voluntarily recalling multiple dark chocolate products because they may contain an undeclared milk allergen.Class II
2017-11-29Dark Chocolate Blueberries 8/7 oz., 8 pc. display, 25 lbs.GKI Foods, LLCGKI Foods of Brighton, Michigan is voluntarily recalling multiple dark chocolate products because they may contain an undeclared milk allergen.Class II
2017-11-29Dark Chocolate Turbinado Sea Salt Almonds , 15 lbs., 10 lbs., 18/14 oz.,GKI Foods, LLCGKI Foods of Brighton, Michigan is voluntarily recalling multiple dark chocolate products because they may contain an undeclared milk allergen.Class II
2017-11-29Dark Chocolate Ginger , 25 lbs., 15 lbs.,GKI Foods, LLCGKI Foods of Brighton, Michigan is voluntarily recalling multiple dark chocolate products because they may contain an undeclared milk allergen.Class II
2017-11-29Dark Chocolate Pineapple, 8/ 8oz., 8 pc/displayGKI Foods, LLCGKI Foods of Brighton, Michigan is voluntarily recalling multiple dark chocolate products because they may contain an undeclared milk allergen.Class II
2017-11-29Dark Chocolate Banana Chips, 25 lbs., 8/8 oz., 8 pc. display,GKI Foods, LLCGKI Foods of Brighton, Michigan is voluntarily recalling multiple dark chocolate products because they may contain an undeclared milk allergen.Class II

All 22 records for GKI Foods, LLC

All 2017 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 access

Recall 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.