Class ITerminated · reported 2025-08-06

Sheehan Brothers Vending BBQ Riblet Sandwich with Coleslaw, 8 oz (226g), in a plastic…

SHEEHAN BROTHERS VENDING recalled this product and the FDA reported the enforcement action on 6 August 2025 as Class I. The recall was initiated by the firm. Undeclared sesame

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
Sheehan Brothers Vending BBQ Riblet Sandwich with Coleslaw, 8 oz (226g), in a plastic tray/2 oz cup and individually wrapped in plastic, UPC: 100000222744
UPC
100000222744
Reason for recall
Undeclared sesame
Firm location
Springfield, Ohio, United States
Classification
Class I
Status
Terminated
Recall number
H-0336-2025
Quantity
209 individual units
Distribution
IN, KY, OH
Initiated
8 July 2025
Reported by FDA
6 August 2025
Terminated
17 September 2025
Firm notified by
Press Release
Product codes
Prepared: Jul 1, 2025 and Sell By: Jul 7, 2025 Prepared: Jul 6, 2025 and Sell By: Jul 12, 2025

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 6 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 6 separate recalls, which almost every published figure does, overstates it by a factor of 6. All 6 of them are listed on this page.
  • The recall ran for 2 months, from 8 July 2025 to termination on 17 September 2025. 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 4 weeks after the firm began the recall.
  • Recalls of a prepared meal or sandwich run a median of 6 months, so this one was shorter than usual for its category. Prepared meals concentrate every other category's hazards into one package: they are assembled from many components, handled after any cook step, sold ready to eat, and carry an ingredient list long enough to lose an allergen in.

Named in the distribution pattern: Indiana, Kentucky, Ohio. 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: sesame.

Filed under prepared meals and sandwiches. A product can sit in more than one.

Every product in this recall

The FDA opened 6 enforcement records for this one recall, one per product code. This page carries all of them; the 5 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.

Other prepared meals and sandwiches 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
2026-09-02Sura Tanmen Hot and Sour Flavor Premium Japanese Noodles & Soup Base. Retail package net wt. 15.4oz. Product is ramen noodle kit which contains noodles and Soba soup packet. Item #05410 retail package, UPC 085315054108 Item #05410.1 cardboard box (12 packages per case), UPC 085315054105 Product is Perishable Frozen or Refrigerated and made by Sun Noodle Hawaii 1933 Colburn Street, Honolulu, HIH & U Inc. dba Sun NoodleSoba sauce packet, which contains bonito, sardine, and mackerel (fish), was packed into Sura Tanmen Hot and Sour Flavor ramen noodle package kit, but fish species are not declared on finished product label.Class I
2026-08-12Spicy Breakfast Burrito sold under the following brand names: FRESH & READY FOODS Spicy Breakfast Burrito Net Wt. 8.2 oz (232g) UPC 1 00001 00029 7 and Sprig & Sprout Spicy Breakfast Burrito IN A SPICY TORTILLA NET WEIGHT 8.3oz (234g) Contains: Egg, Milk, Wheat. MG Foods Charlotte, NC 28272M.G. Foods, Inc.Undeclared Soy. The firm received complaints of sausage in the burritos. Upon review the firm discovered the sausage contains soy which is not listed on the label.Class I
2026-08-12Blank Slate Creamery VEGAN NON-DAIRY FROZEN DESSERT COCONUT FUDGE SANDWICHES, 4.5 oz clear plastic packageBlank Slate Creamery Productionundeclared eggClass I
2026-07-01El David Gelee, Bonbons with fruits Soft & Juicy, 400g. Packaged in decorated paperboard box and covered entirely in transparent, flexible plastic wrap. (20 bonbon pieces per 400g box). UPC 5304000050757Alb-USA Enterprises IncUndeclared colors (FD&C Yellow 5 and FD&C Red 40).Class II
2026-06-17Individual Unit Label (both lid and front of cup): Whole Foods Market Kitchens Minestrone Soup, VEGETARIAN NET WT 24 OZ (1 Lb 8OZ) 680g. Case Label: Whole Foods Global Minestrone Soup 702505, KEEP REFRIGERATED, Distributed by Whole Foods Market Austin, TX 78703. Eight (8)/ 24 oz. Cups (Net Wt. 12 LBS)/case.Kettle Cuisine, LLCContains undeclared allergen (shrimp).Class I
2026-06-17Park St. Deli Macaroni & Cheese, NET WT 20 OZ (1 LB 4 OZ) 567g, product packed in plastic tub and placed into paperboard sleeve. 9/20 oz packages per case.BEF Foods, IncUndeclared allergen (soy lecithin).Class II
2026-06-10UPC 21494500000 Ready Meals MEAL SALMON With LEMON CAPELLINI PASTA SS This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.Albertsons Companies LLCContains statement does not declare SalmonClass III
2026-06-10UPC 21788400000 Ready Meals SANDWICH TUNA SALAD CROISSANT SS COLD This is Albertson's store-made item and sold by unit at point of sale with grocery store's scale label.Albertsons Companies LLCContains statement does not declare TUNAClass III

Other records from SHEEHAN BROTHERS VENDING

The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 5 other records name this firm.

All 6 records for SHEEHAN BROTHERS VENDING

All 2025 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.