CLASS II Food recall · Reported 20 Dec 2023 · FDA Enforcement Report

Gaw's Classic Italian sub, Foam Tray package recalled

Gaws Gourmet Foods is recalling Gaw's Classic Italian sub, Foam Tray package, distributed in Michigan. The recall was initiated on 29 Nov 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUse By 11-28-23 thru 12-15-23
Quantity recalled699 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-0658-2024
FDA event ID
93517
Recalling firm
Gaws Gourmet Foods, Marysville, MI
Brand
Gaw's
Classification
Class II
Status
Terminated
Recall initiated
29 Nov 2023
FDA classified
27 Dec 2023
Reported
20 Dec 2023
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Sesame
Product category
Ready Meals

Timeline

29 Nov 2023Recall initiated by company
20 Dec 2023Published in enforcement report+21 days
27 Dec 2023Classified by FDA+7 days

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

Reason for recall

undeclared sesame

Product as listed by the FDA

Gaw's Classic Italian sub 8oz, Foam Tray with Clear Plastic Wrap package, UPC:1725600920

Where it was distributed

MI

Michigan

Questions about this recall

Is Gaw's Classic Italian sub, Foam Tray package recalled?

Yes. Gaws Gourmet Foods recalled Gaw's Classic Italian sub, Foam Tray package on 29 Nov 2023. The recall is Class II and its status is Terminated. Recall number F-0658-2024.

Why was it recalled?

undeclared sesame

Which lots are affected?

Use By 11-28-23 thru 12-15-23

Where was it sold?

MI

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

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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