Dark Chocolate Almond Bark 10 oz.,10 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 Almond Bark 10 oz.,10 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-0316-2018

Quantity

1,517 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

All products manufactured between 01/14/16 to 10/24/17; Lots: Lot# 01916B Lot# 04216 Lot# 08916 Lot# 10216 Lot# 13216B Lot# 16016B Lot# 19316B Lot# 19416B Lot# 22316 Lot# 26016 Lot# 26316 Lot# 30516 Lot# 30616 Lot# 30616 Lot# 27516B Lot# 31416 Lot# 32016 Lot# 35416B Lot# 35516 Lot# 10817B Lot# 11617 Lot# 11617 Lot# 12917 Lot# 15917 Lot# 17117 Lot# 19317 Lot# 19417 Lot# 21917B Lot# 23417 Lot# 27617B Lot# 27917 Lot# 04216 Lot# 08216B Lot# 08216B Lot# 10216 Lot# 10216B Lot# 13216B Lot# 13816 Lot# 20916 Lot# 20916 Lot# 22316 Lot# 22316 Lot# 25616B Lot# 25816 Lot# 25816B Lot# 25916 Lot# 25916B Lot# 26016 Lot# 27516B Lot# 30616 Lot# 33516 Lot# 34916 Lot# 35016 Lot# 01817 Lot# 02317 Lot# 04617 Lot# 19417 Lot# 19417 Lot# 19517 Lot# 19817 Lot# 19917 Lot# 20117 Lot# 20517 Lot# 08216B Lot# 08916 Lot# 00616B Lot# 01916B Lot# 06016 Lot# 08216B Lot# 10216B Lot# 10216B Lot# 13216B Lot# 13816 Lot# 13816 Lot# 16016B Lot# 18016 Lot# 18116 Lot# 20016 Lot# 20716B Lot# 20916 Lot# 23516 Lot# 23916 Lot# 27516B Lot# 32016 Lot# 33516 Lot# 33516 Lot# 34916 Lot# 35016 Lot# 35516 Lot# 35516B Lot# 05517 Lot# 05917B Lot# 06217 Lot# 06517 Lot# 06517 Lot# 09417 Lot# 09417 Lot# 10817B Lot# 12917 Lot# 15917 Lot# 18617 Lot# 19317 Lot# 20517 Lot# 21217B Lot# 21917B Lot# 23417 Lot# 24817 Lot# 25117 Lot# 26517B Lot# 04216 Lot# 05616 Lot# 06016 Lot# 19416B Lot# 19516 Lot# 20016 Lot# 22316B Lot# 23316 Lot# 23516 Lot# 26416B Lot# 27516B Lot# 34916 Lot# 35016 Lot# 01317 Lot# 01817 Lot# 02317 Lot# 05517 Lot# 09417 Lot# 17117 Lot# 18617 Lot# 26517B Lot# 27917 Lot# 29217 Lot# 26316 Lot# 24817 Lot# 25017

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

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.

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.

All 22 records for GKI Foods, LLC

All 2017 recalls · All FDA food recall data