CLASS I Food recall · Reported 11 Jan 2017 · FDA Enforcement Report

Buffalo Chicken Sandwich Deli Selections Ingredients recalled

Derby City Vending is recalling Buffalo Chicken Sandwich Deli Selections Ingredients: Chicken***Ranch Cup, distributed in Indiana, Kentucky. The recall was initiated on 2 Dec 2016 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesFresh Thru 10/31/16 t0 12/04/16
Quantity recalled35

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-1143-2017
FDA event ID
75849
Recalling firm
Derby City Vending, Louisville, KY
Brand
Buffalo
Classification
Class I
Status
Terminated
Recall initiated
2 Dec 2016
FDA classified
3 Jan 2017
Reported
11 Jan 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
Ready Meals

Timeline

2 Dec 2016Recall initiated by company
3 Jan 2017Classified by FDA+32 days
11 Jan 2017Published in enforcement report+8 days

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

Reason for recall

The firm failed to declare milk, egg & soy on their label.

Product as listed by the FDA

Derby City Vending Buffalo Chicken Sandwich Deli Selections Ingredients: Chicken***Ranch Cup; Pretzel bun***Lettuce, Tomato CONTAINS WHEAT Fresh Thru 12/4/16 Derby City Vending Louisville, KY 40206

Where it was distributed

Product was shipped to IN & KY.

IndianaKentucky

Questions about this recall

Why was it recalled?

The firm failed to declare milk, egg & soy on their label.

Which lots are affected?

Fresh Thru 10/31/16 t0 12/04/16

Where was it sold?

Product was shipped to IN & KY.

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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