Class ITerminated · reported 2016-09-07

All American Burger Product ID 470007, C47007

Let's Do Lunch, Inc. recalled this product and the FDA reported the enforcement action on 7 September 2016 as Class I. The recall was initiated by the firm. Potential Listeria monocytogenes contamination.

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 American Burger Product ID 470007, C47007
Reason for recall
Potential Listeria monocytogenes contamination.
Recalling firm
Let's Do Lunch, Inc.
Firm location
Gardena, California, United States
Classification
Class I
Status
Terminated
Recall number
F-2033-2016
Quantity
590 cases
Distribution
U.S. distribution to the following; CA, NM, OH, VA, AZ, MI, TX, NC, PA. No foreign distribution.
Initiated
25 July 2016
Reported by FDA
7 September 2016
Terminated
31 May 2017
Firm notified by
Letter
Product codes
Lot #052016D, 052516C, 060916C, 061016C

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 9 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 9 separate recalls, which almost every published figure does, overstates it by a factor of 9. 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 9 of them.
  • The recall ran for 10 months, from 25 July 2016 to termination on 31 May 2017. 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 8 states, and the FDA published the enforcement report 6 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.

Named in the distribution pattern: California, New Mexico, Ohio, Virginia, Arizona, Michigan, Texas, North Carolina. 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.

Other records from Let's Do Lunch, Inc.

The FDA opens one enforcement record per product code, so several of these are frequently one recall event. 47 other records name this firm.

ReportedProductFirmReasonClass
2016-09-07Beef Sausage Breakfast Sandwich Product ID C99018Let's Do Lunch, Inc.Potential Listeria monocytogenes contamination.Class I
2016-09-07Beef Sausage & Cheese Mini Bagel Sandwich Product ID C80916Let's Do Lunch, Inc.Potential Listeria monocytogenes contamination.Class I
2016-09-07Cheeseburger Sliders Product ID C47220, 470220Let's Do Lunch, Inc.Potential Listeria monocytogenes contamination.Class I
2016-09-07BBQ Rib Sandwich Product ID C46007, 460007Let's Do Lunch, Inc.Potential Listeria monocytogenes contamination.Class I
2016-09-07Chicken Patty Sandwich on a Whole Grain Bun Product ID 400003Let's Do Lunch, Inc.Potential Listeria monocytogenes contamination.Class I
2016-09-07All American Cheeseburger Product ID 470007Let's Do Lunch, Inc.Potential Listeria monocytogenes contamination.Class I
2016-09-07Chili Dog, Low Fat/Low Sodium Product ID 952000Let's Do Lunch, Inc.Potential Listeria monocytogenes contamination.Class I
2016-09-07Chicken Double Dogs on Whole Grain Bun Product ID 809021Let's Do Lunch, Inc.Potential Listeria monocytogenes contamination.Class I
2016-08-17Integrated Food Service Turkey Breast & Cheese Sandwich on a Whole Grain French Roll Code #C16001/160001Let's Do Lunch, Inc.Potential Listeria monocytogenes contamination.Class I
2016-08-17Cafe Favorites Oven Roasted Turkey Breast & Cheese Deli Flatz-IW Code #C22348/22348Let's Do Lunch, Inc.Potential Listeria monocytogenes contamination.Class I

All 48 records for Let's Do Lunch, Inc.

All 2016 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.