CLASS I Food recall · Reported 17 May 2017 · FDA Enforcement Report

7-eleven Caesar Side Salad recalled by Del Monte Fresh Produce N.A.

Del Monte Fresh Produce N.A., Inc. HQ is recalling 7-eleven Caesar Side Salad, distributed in Colorado. The recall was initiated on 13 Apr 2017 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesBest By 4/17/17; UPC 0 52548 59414 5; Lot 07101101
Quantity recalled740 units

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-2204-2017
FDA event ID
77015
Recalling firm
Del Monte Fresh Produce N.A., Inc. HQ, Coral Gables, FL
Classification
Class I
Status
Terminated
Recall initiated
13 Apr 2017
FDA classified
8 May 2017
Reported
17 May 2017
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Milk
Product category
Salad Kits

Timeline

13 Apr 2017Recall initiated by company
8 May 2017Classified by FDA+25 days
17 May 2017Published in enforcement report+9 days

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

Reason for recall

Undeclared milk, eggs, wheat and fish (anchovies).

Product as listed by the FDA

7-ELEVEN CAESAR SIDE SALAD 3 oz. packaged in clear plastic container

Where it was distributed

The product is sold only in 7-11 stores in Colorado.

Colorado

Stores named: 7-Eleven

Questions about this recall

Why was it recalled?

Undeclared milk, eggs, wheat and fish (anchovies).

Which lots are affected?

Best By 4/17/17; UPC 0 52548 59414 5; Lot 07101101

Where was it sold?

The product is sold only in 7-11 stores in Colorado.

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 26 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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