Class ITerminated · reported 2016-03-30

Dark Chocolate Covered Coffee Beans, packaged in 12 oz. tubs

Lipari Foods, Inc. recalled this product and the FDA reported the enforcement action on 30 March 2016 as Class I. The recall was initiated by the firm. Lipari Foods, LLC has issued a voluntary recall of dark chocolate covered coffee beans packaged by sister company JLM due to an undeclared allergen of tree nuts (almonds).

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 Covered Coffee Beans, packaged in 12 oz. tubs
Reason for recall
Lipari Foods, LLC has issued a voluntary recall of dark chocolate covered coffee beans packaged by sister company JLM due to an undeclared allergen of tree nuts (almonds).
Recalling firm
Lipari Foods, Inc.
Firm location
Warren, Michigan, United States
Classification
Class I
Status
Terminated
Recall number
F-0776-2016
Quantity
26 cases  477308 (Tub LG Dark Chocolate Coffee Beans 12-12oz) & 17 cases  510526 (Tub LG PL Dark Chocolate Coffee Beans 12-12oz)
Distribution
Domestic: Indiana, Kentucky, Michigan, Ohio, Pennsylvania, Tennessee, Wisconsin and West Virginia. Foreign: None VA/DOD: None
Initiated
23 February 2016
Reported by FDA
30 March 2016
Terminated
8 February 2017
Firm notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product codes
Dark Chocolate Covered Coffee Beans, packaged in 12 oz. tubs; (Multiple Brands including: Angeli Foods, Hardings Markets, Goosberries Fresh Food Market, Marthas Vineyard, Hollywood Market, Daniels Foods, Snooks Butcher Shoppe, Martins, Holiday Market, The Purple Onion, Remke Market) Lipari Product Number 510526, Lot # 22201512, Weight 12oz Tubs, Best By Date: 12/21/16, UPC # 094776131761; and Generic brand Lipari Product Number 477308, Lot # 22201512, Weight 12oz Tubs, Best By Date: 12/21/16, and UPC # 094776131761.

Reading this record

Five things about this record are not in the record itself, and each one changes how it should be read.

  • Class I means the FDA judged a reasonable probability that the product would cause serious health consequences or death. 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 record is the only one the FDA opened for its recall event, so it covers a single product code.
  • The recall ran for 12 months, from 23 February 2016 to termination on 8 February 2017. 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 a snack or confectionery product run a median of 7 months, so this one was longer than usual for its category. Snacks and confectionery recall for allergens more than for anything else, because a chocolate or a coated snack passes through shared equipment carrying milk, soy and nuts, and the label is the only control between them and the consumer.

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: tree nuts.

Filed under snacks and confectionery and beverages and juice. A product can sit in more than one.

Other snacks and confectionery 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
2026-09-02ERIDANOUS GREEK STYLE Shortbread Cookies with Chocolate Truffle Coating & Apricot Filling. Product is packed onto a plastic carton tray with outer paper sleeve, 330 g (weight), UPC: 4056489125839.Lidl US TRADINGThe firm discovered that certain units shipped to the U.S. retail stores only has "foreign languages" on the label. Product has undeclared wheat, soy, milk, eggs and tree nut (coconut).Class II
2026-08-19Dark Chocolate Coconut Almond Bites, 3.17oz, Plastic Pouches, 10 Packages per case.Bazzini LLCUndeclared peanutsClass I
2026-08-19Lyle Style Mild Bloody Mary Mix, 32oz. glass bottle. UPC code 7 84762 03730 3. The label declares "***Ingredients***Tomato Juice ***lemon***Worcestershire sauce (vinegar, molasses, water, corn sweeteners, caramel coloring, anchovies, natural flavorings)***Made in the Columbia River Gorge - Lyle, Washington***"Lyle StyleUndeclared Soy. Finished product ingredients statement declares Worcestershire sauce but does not declare sub-ingredients Soy Flavoring and Soy Lecithin.Class II
2026-08-12Blank Slate Creamery VEGAN NON-DAIRY FROZEN DESSERT COCONUT FUDGE SANDWICHES, 4.5 oz clear plastic packageBlank Slate Creamery Productionundeclared eggClass I
2026-07-22Ice Pop, D'Dioses Nuez, 1 Bar (81.7 g), with UPC 827912008548D'Dioses Fruit Pops, Inc.May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.Class I
2026-07-22Ice Pop, D'Dioses Tamarindo, 1 Bar (81.7 g), with UPC 827912008593D'Dioses Fruit Pops, Inc.May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.Class I
2026-07-22Ice Pop, D'Dioses Cookies Cream, 1 Bar (81.7 g), with UPC 710594511362D'Dioses Fruit Pops, Inc.May contain undeclared milk, pecans, pistachios, yellow #5 and red #40.Class 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

Other records from Lipari Foods, Inc.

The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 79 other records name this firm.

ReportedProductFirmReasonClass
2018-08-15Premo Brand and Fresh Grab turkey and Swiss submarine sandwiches, 4/6 oz, and 18/6 oz.Lipari Foods, Inc.Lipari Foods, LLC has issued a voluntary recall of Premo Brand and Fresh Grab turkey and Swiss submarine sandwiches produced and packaged by sister company JLM due to potential contamination of Listeria monocytogenesClass I
2017-10-04Sunflower Seeds Honey Roasted, 12oz Tubs & 25lb BulkLipari Foods, Inc.Lipari Foods LLC initiated a voluntary recall of Honey Roasted Sunflower Seeds, 12oz Tubs & 25lb Bulk, due to an off taste following a consumer complaint and mislabeled shelf life.Class III
2017-04-12Thortons Italian Footlong 6/12 oz.Lipari Foods, Inc.JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.Class I
2017-04-12Thortons Italian & Provolone 12 oz.Lipari Foods, Inc.JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.Class I
2017-04-12Premo Turkey & Garlic Mayo Item # 207455, Net wt. 5.5 oz; Core-Mark Turkey & Garlic Mayo Item # 568207, Net wt. 5.5 oz; Fresh Grab Turkey & Provolone with Garlic Mayo Item # 455956, Net wt. 5.5 ozLipari Foods, Inc.JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.Class I
2017-04-12Premo Signature Classic Italian, 1/6 oz.Lipari Foods, Inc.JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.Class I
2017-04-12Premo Asiago Italian Item # 207919, Net Wt 6 oz; Fresh Grab Asiago Italian Item # 251847, Net Wt 6 oz; Core-Mark Asiago Italian Item # 568377, Net Wt 6 oz;Lipari Foods, Inc.JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.Class I
2017-04-12Premo Ham & Provolone Item # 207851, Net Wt 6 oz; Fresh Grab Ham & Provolone Item # 251745, Net Wt 6 oz; Core-Mark Ham & Provolone Item # 568343, Net Wt 6 oz;Lipari Foods, Inc.JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.Class I
2017-04-12Premo Italian Wrap, 1/5 oz.Lipari Foods, Inc.JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.Class I
2017-04-12Coffee House Italian Flatbread , Item # 226323 net wt. 6 oz.; Fresh Grab Italian Flatbread , Item # 252323 net wt. 6 oz.Lipari Foods, Inc.JLM Manufacturing initiated a recall on 02/21/2017 of multiple ready to eat sandwiches containing cheese because of a supplier's recall of cheese due to Listeria monocytogenes.Class I

All 80 records for Lipari Foods, Inc.

All 2016 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.