Class ITerminated · reported 2015-02-11

CARROLL SHELBY'S ORIGINAL TEXAS BRAND CHILI KIT, NET WT. 4 oz. (113 g), Dist.

Reily Foods Co. recalled this product and the FDA reported the enforcement action on 11 February 2015 as Class I. The recall was initiated by the firm. Kits contain peanut and almond allergens that are not declared on the products' ingredient statements.

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
CARROLL SHELBY'S ORIGINAL TEXAS BRAND CHILI KIT, NET WT. 4 oz. (113 g), Dist. by Reily Foods Company, New Orleans, LA 70130, 1-800-535-1961, UPC 0-00-72396-10000-8
UPC
00072396100008
Reason for recall
Kits contain peanut and almond allergens that are not declared on the products' ingredient statements.
Recalling firm
Reily Foods Co.
Firm location
New Orleans, Louisiana, United States
Classification
Class I
Status
Terminated
Recall number
F-0956-2015
Quantity
3,189,976 units
Distribution
Nationwide.
Initiated
18 December 2014
Reported by FDA
11 February 2015
Terminated
21 April 2015
Firm notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Product codes
Best by: July 1, 2016 - Nov 21, 2016

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 4 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 4 separate recalls, which almost every published figure does, overstates it by a factor of 4. 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 4 of them.
  • The recall ran for 4 months, from 18 December 2014 to termination on 21 April 2015. 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 8 weeks after the firm began the recall.
  • The product description on this record names no food this site can classify, so it appears on no food-type page. That is a limit of the description rather than of the recall.

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: peanuts, tree nuts.

Other records from Reily Foods Co.

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

ReportedProductFirmReasonClass
2016-03-16CARROLL SHELBY'S(R) ORIGINAL TEXAS BRAND White CHICKEN CHILI KIT, NET WT 3 OZ (85g), DIST. BY REILY FOODS COMPANY, NEW ORLEANS, LA 70130, UPC 7239610019Reily Foods Co.Cartons of Carroll Shelby White Chicken Chili (3oz retail carton) produced before 03/03/2015 state that the sodium per serving was 0 mg, the correct amount is 590 mg per serving.Class II
2015-10-14Blue Plate(R) LIGHT MAYONNAISE, 18 Fl OZ (1 PT 2 OZ) 532, mL. UPC 47900-50638Reily Foods Co.One lot of Blue Plate Light Mayonnaise has the Blue Plate Mayonnaise ingredient statement and nutrition facts on the rear panel.Class III
2015-02-11WICK FOWLER'S FAMOUS TEXAS STYLE 2-ALARM Chili Kit, NET WT. 3.6525 oz. (102g), Dist. by Reily Foods Company, New Orleans, LA 70130, 1-800-535-1961, UPC 0-00-71092-00069-8Reily Foods Co.Kits contain peanut and almond allergens that are not declared on the products' ingredient statements.Class I
2015-02-11CARROLL SHELBY'S ORIGINAL TEXAS BRAND WHITE CHICKEN CHILI KIT, 3 oz. (85 g), Dist. by Reily Foods Company, New Orleans, LA 70130, UPC 0-00-72396-10019-0Reily Foods Co.Kits contain peanut and almond allergens that are not declared on the products' ingredient statements.Class I
2015-02-11WICK FOWLER'S TEXAS STYLE FALSE ALARM Mild Chili Kit, NET WT. 3.03 oz. (86g), Dist. by Reily Foods Company, New Orleans, LA 70130, UPC 0-00-71092-00111-4Reily Foods Co.Kits contain peanut and almond allergens that are not declared on the products' ingredient statements.Class I

All 6 records for Reily Foods Co.

All 2015 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.