CLASS I Food recall · Reported 7 Sep 2016 · FDA Enforcement Report

All American Burger Product ID 470007, C47007 recalled by Let's Do Lunch

Let's Do Lunch is recalling All American Burger Product ID 470007, C47007, distributed in 9 states. The recall was initiated on 25 Jul 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot #052016D, 052516C, 060916C, 061016C
Quantity recalled590 cases

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-2033-2016
FDA event ID
74873
Recalling firm
Let's Do Lunch, Gardena, CA
Classification
Class I
Status
Terminated
Recall initiated
25 Jul 2016
FDA classified
31 Aug 2016
Reported
7 Sep 2016
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Listeria
Product category
Other

Timeline

25 Jul 2016Recall initiated by company
31 Aug 2016Classified by FDA+37 days
7 Sep 2016Published in enforcement report+7 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Potential Listeria monocytogenes contamination.

Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.

Product as listed by the FDA

All American Burger Product ID 470007, C47007

Where it was distributed

U.S. distribution to the following; CA, NM, OH, VA, AZ, MI, TX, NC, PA. No foreign distribution.

ArizonaCaliforniaMichiganNorth CarolinaNew MexicoOhioPennsylvaniaTexasVirginia

Questions about this recall

Is All American Burger Product ID 470007, C47007 recalled?

Yes. Let's Do Lunch recalled All American Burger Product ID 470007, C47007 on 25 Jul 2016. The recall is Class I and its status is Terminated. Recall number F-2033-2016.

Why was it recalled?

Potential Listeria monocytogenes contamination.

Which lots are affected?

Lot #052016D, 052516C, 060916C, 061016C

Where was it sold?

U.S. distribution to the following; CA, NM, OH, VA, AZ, MI, TX, NC, PA. No foreign distribution.

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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