CLASS I Food recall · Reported 13 Oct 2021 · FDA Enforcement Report

Earle of Sandwiches Mild Smoked Jalapeno Sub recalled

The Earl of Sandwiches is recalling Earle of Sandwiches Mild Smoked Jalapeno Sub, Smoked Jalapeno Sausage and Peperjack, distributed in Minnesota, Utah, Washington. The recall was initiated on 16 Sep 2021 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesSandwiches Purchased before 9/15/2021
Quantity recalled2776 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-0001-2022
FDA event ID
88744
Recalling firm
The Earl of Sandwiches, Willernie, MN
Brand
Earle
Classification
Class I
Status
Terminated
Recall initiated
16 Sep 2021
FDA classified
1 Oct 2021
Reported
13 Oct 2021
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Egg
Product category
Ready Meals

Timeline

16 Sep 2021Recall initiated by company
1 Oct 2021Classified by FDA+15 days
13 Oct 2021Published in enforcement report+12 days

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

Reason for recall

Sandwiches may contain undeclared soy and egg.

Product as listed by the FDA

Earle of Sandwiches Mild Smoked Jalapeno Sub, Smoked Jalapeno Sausage and Peperjack Cheese on Parmasan Crusted French Bread. Net Wt. 7oz (198g), UPC 97256 75671, Keep Refrigerated. Earle of Sandwiches, Willernie, MN 55090

Where it was distributed

MN, UT, WA

MinnesotaUtahWashington

Questions about this recall

Why was it recalled?

Sandwiches may contain undeclared soy and egg.

Which lots are affected?

Sandwiches Purchased before 9/15/2021

Where was it sold?

MN, UT, WA

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.

Other products in this recall event

4 other products · FDA event 88744

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