CLASS II Food recall · Reported 31 May 2023 · FDA Enforcement Report

Turkey and Havarti Sandwich recalled by Garden Highway Southwest, LLC

Garden Highway Southwest, LLC (Ghsw, LLC) is recalling Turkey and Havarti Sandwich, distributed in Kansas, Louisiana, Missouri, Nebraska, Texas. The recall was initiated on 25 Apr 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesAll sell-by dates up to and including 4/29/23; GHSW 001 - GHSW 114
Quantity recalled16,866 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-0935-2023
FDA event ID
92211
Classification
Class II
Status
Terminated
Recall initiated
25 Apr 2023
FDA classified
24 May 2023
Reported
31 May 2023
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Sesame
Product category
Ready Meals

Timeline

25 Apr 2023Recall initiated by company
24 May 2023Classified by FDA+29 days
31 May 2023Published 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

Undeclared sesame allergen

Product as listed by the FDA

Turkey and Havarti Sandwich Net Wt 8.55 oz (242g) UPC 826766155842 packaged in plastic clamshell container

Where it was distributed

KS, NE, MO, LA, TX

KansasLouisianaMissouriNebraskaTexas

Questions about this recall

Why was it recalled?

Undeclared sesame allergen

Which lots are affected?

All sell-by dates up to and including 4/29/23; GHSW 001 - GHSW 114

Where was it sold?

KS, NE, MO, LA, TX

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 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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