Class ITerminated · reported 2023-10-04

Coffee Dessert Cups; parve; 6 PACK / SINGLE; UPC: 0-91404-15313-3

ICE CREAM HOUSE recalled this product and the FDA reported the enforcement action on 4 October 2023 as Class I. The recall was initiated by the firm. Products may be contaminated with Listeria monocytogenes.

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
Coffee Dessert Cups; parve; 6 PACK / SINGLE; UPC: 0-91404-15313-3
UPC
091404153133
Reason for recall
Products may be contaminated with Listeria monocytogenes.
Recalling firm
ICE CREAM HOUSE
Firm location
Brooklyn, New York, United States
Classification
Class I
Status
Terminated
Recall number
F-1680-2023
Quantity
N/A
Distribution
OH, NJ, NY
Initiated
22 August 2023
Reported by FDA
4 October 2023
Terminated
14 June 2024
Firm notified by
Telephone
Product codes
No 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 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 is one of 80 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 80 separate recalls, which almost every published figure does, overstates it by a factor of 80. 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 80 of them.
  • The recall ran for 10 months, from 22 August 2023 to termination on 14 June 2024. 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 3 states, and the FDA published the enforcement report 6 weeks after the firm began the recall.
  • Recalls of a beverage or juice run a median of 6 months, so this one was longer than usual for its category. Juice is the other food with its own HACCP regulation in the United States, 21 CFR part 120, which requires a treatment achieving a 5-log reduction of the pertinent pathogen, and unpasteurised juice recalls are almost always a failure of that step or an exemption misapplied.

Named in the distribution pattern: Ohio, New Jersey, New York. 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

Listeria monocytogenes

Listeria monocytogenes is a bacterium that grows at refrigeration temperature, which is why it dominates recalls of ready-to-eat foods that are never cooked again before they are eaten.

A preventive controls plan covers Listeria contamination 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)(3)
Sanitation controls: the controls on cleaning food-contact surfaces and on preventing cross-contact and cross-contamination from insanitary objects, people and equipment.
21 CFR 117.165(a)(3)
Environmental monitoring: testing the processing environment for an environmental pathogen, required when a ready-to-eat food is exposed to the environment before packaging.
21 CFR 117.150
Corrective actions: what a facility does when a preventive control was not properly implemented, including identifying and correcting the problem and evaluating the food for safety.

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

Other beverages and juice 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
2025-02-12item 8201864 JUST BAKED COFFEE ROLLS 78x3OZ, NET WT 14.62 LBFGF, LLCpotential for contamination with listeria monocytogenesClass II
2025-02-12item 8201901 JUST BAKED APPLE CIDER CAKE RINGS WITH NATURAL FLAVORS 144x2.5OZ, NET WT 22.5 LBFGF, LLCpotential for contamination with listeria monocytogenesClass II
2024-08-07Dolcezza Hot Cocoa Gelato 16 fl oz/1 pint, UPC 857838006610. Packaged in paper containers, 8 containers per case.Totally Cool, Inc.Possible contamination with Listeria monocytogenesClass II
2024-08-07Marco Green Tea White Chocolate Ice Cream 16 fl oz/1 pint, UPC 860006880521. Packaged in paper containers, 8 containers per case.Totally Cool, Inc.Possible contamination with Listeria monocytogenesClass II
2024-08-07Dolcezza Coffee & Cookies Gelato 16 fl oz/1 pint, UPC 857838006038. Packaged in paper containers, 8 containers per case.Totally Cool, Inc.Possible contamination with Listeria monocytogenesClass II
2023-12-20Wilcox Premium Coffee Heath Bar in 1.5QT, Quart, Pint, and 3 Gallon sizesWILCOX ICE CREAMProducts may be contaminated with Listeria monocytogenes.Class I
2023-12-20Wilcox Premium Coffee; 4 oz Cup; UPC 04372600403; Wilcox Premium Coffee in 1.5QT, Quart, Pint, 3 Gallon, and 1 Gallon sizesWILCOX ICE CREAMProducts may be contaminated with Listeria monocytogenes.Class I
2023-12-20Wilcox Premium Cream and Coffee Fudge in 1.5QT, Quart, and Pint sizesWILCOX ICE CREAMProducts may be contaminated with Listeria monocytogenes.Class I

Other records from ICE CREAM HOUSE

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
2023-10-04Mini Sorbet Pops; parve; 7 PACK / SINGLE; UPC: 0-91404-15305-8ICE CREAM HOUSEProducts may be contaminated with Listeria monocytogenes.Class I
2023-10-04Tropical Flute / Pre-Cut 12 Slices; parve; 1 PACK; UPC: 0-91404-15243-3ICE CREAM HOUSEProducts may be contaminated with Listeria monocytogenes.Class I
2023-10-04{P} Strawberry Shortcake Roll; parve; 1 PACK / SINGLE; UPC: 0-91404-15298-0ICE CREAM HOUSEProducts may be contaminated with Listeria monocytogenes.Class I
2023-10-04Mini Dippers Ice Cream; parve; 6 PACK / SINGLE; UPC: 0-91404-15289-1ICE CREAM HOUSEProducts may be contaminated with Listeria monocytogenes.Class I
2023-10-04Mini Sorbet Cake Blueberry / Lime; parve; 1 PACK; UPC: 0-91404-15219-8ICE CREAM HOUSEProducts may be contaminated with Listeria monocytogenes.Class I
2023-10-04Mini Ice Cream Lollies; dairy / parve; 12 PACK / SINGLE; UPC: 0-91404-15110-8ICE CREAM HOUSEProducts may be contaminated with Listeria monocytogenes.Class I
2023-10-04Premium Sorbet Trifle Medium; parve; 1 PACK; UPC: 0-91404-15164-1 and Premium Sorbet Trifle; Small; parve; 1 PACK; UPC: 0-91404-15165-8ICE CREAM HOUSEProducts may be contaminated with Listeria monocytogenes.Class I
2023-10-048' Sorbet Cake Strawberry/Mango; parve; 1 PACK; UPC: 0-91404-15429-1 and Mini Sorbet Cake Strawberry / Mango; parve; 1 PACK; UPC: 0-91404-15132-0ICE CREAM HOUSEProducts may be contaminated with Listeria monocytogenes.Class I
2023-10-04Cup Cake Party; dairy / parve; 6 PACK / SINGLE; UPC: 0-91404-15287-7ICE CREAM HOUSEProducts may be contaminated with Listeria monocytogenes.Class I
2023-10-0410' Hello Kitty Cake; dairy / parve; 1 PACK; UPC: 0-91404-15174-0 and 8' Hello Kitty Cake; dairy / parve; 1 PACK; UPC: 0-91404-15175-7 and 6' Hello Kitty Cake; dairy / parve; 1 PACK; UPC: 0-91404-15176-4ICE CREAM HOUSEProducts may be contaminated with Listeria monocytogenes.Class I

All 80 records for ICE CREAM HOUSE

All 2023 recalls · All FDA food recall data

21 CFR 117.135(c)(3) 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.