Class IITerminated · reported 2020-10-28

All Natural Chocolate Pecan ice cream, 2.5 gallons, UPC:7525200120. Packaged in a…

Homestead Creamery, Inc. recalled this product and the FDA reported the enforcement action on 28 October 2020 as Class II. The recall was initiated by the firm. Undeclared Pecans

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
All Natural Chocolate Pecan ice cream, 2.5 gallons, UPC:7525200120. Packaged in a plastic container
UPC
7525200120
Reason for recall
Undeclared Pecans
Firm location
Wirtz, Virginia, United States
Classification
Class II
Status
Terminated
Recall number
F-0113-2021
Quantity
3 units
Distribution
Distributed to retailers and distributors in Virginia and North Carolina
Initiated
17 September 2020
Reported by FDA
28 October 2020
Terminated
11 January 2022
Firm notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product codes
Best by August 6, 2021 and Best by September 2, 2021

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 2 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 2 separate recalls, which almost every published figure does, overstates it by a factor of 2. All 2 of them are listed on this page.
  • The recall ran for 16 months, from 17 September 2020 to termination on 11 January 2022. 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 6 weeks after the firm began the recall.
  • Recalls of ice cream or frozen dessert run a median of 7 months, so this one was longer than usual for its category. Ice cream and frozen desserts are ready to eat and never cooked again, and freezing preserves Listeria rather than killing it, which is why a positive environmental sample in a frozen dessert plant becomes a recall rather than a corrective action.

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 ice cream and frozen desserts, milk and dairy, nuts and seeds and snacks and confectionery. A product can sit in more than one.

Every product in this recall

The FDA opened 2 enforcement records for this one recall, one per product code. This page carries all of them; the 1 below each have their own page with that product’s lot codes and distribution, and search engines are pointed here for the recall as a whole.

The other 1 records of FDA event 86436
ReportedProductFirmReasonClass
2020-10-28Chocolate Ice Cream, 1 quart, UPC:87525200107. Packaged in paper quart container.Homestead Creamery, Inc.Product mis-packaging; causing undeclared pecans.Class I

Other ice cream and frozen desserts 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 Homestead Creamery, Inc.

The FDA opens one enforcement record per product code, so several of these are frequently one recall event.

ReportedProductFirmReasonClass
2020-12-09Lemonade 1/2 gallon glass bottle. UPC:7525200265. "10% Real Juice Lemonade"Homestead Creamery, Inc.Possible contamination with chlorine sanitizerClass II
2020-10-28Chocolate Ice Cream, 1 quart, UPC:87525200107. Packaged in paper quart container.Homestead Creamery, Inc.Product mis-packaging; causing undeclared pecans.Class I
2020-05-06Homestead Creamery Unsalted Butter. 0.45 lb. net weight. 1 unit per package, cellophane wrapHomestead Creamery, Inc.Unsalted butter has potential to be contaminated with Listeria monocytogenes.Class I

All 4 records for Homestead Creamery, Inc.

All 2020 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.