CLASS I Food recall · Reported 21 Feb 2024 · FDA Enforcement Report

Mexican Style Quinoa Salad recalled by Hans Kissle Company

Hans Kissle Company is recalling Mexican Style Quinoa Salad, distributed in Massachusetts, Maine, New Hampshire, New York, Vermont. The recall was initiated on 17 Jan 2024 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUSE BY 1/22/24 UPC Codes: 0 36217 17201 8
Quantity recalled449 lbs (171cases)

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-0903-2024
FDA event ID
93838
Recalling firm
Hans Kissle Company, Haverhill, MA
Classification
Class I
Status
Terminated
Recall initiated
17 Jan 2024
FDA classified
19 Feb 2024
Reported
21 Feb 2024
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Egg
Product category
Salad Kits

Timeline

17 Jan 2024Recall initiated by company
19 Feb 2024Classified by FDA+33 days
21 Feb 2024Published in enforcement report+2 days

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

Reason for recall

contains undeclared soy and egg

Product as listed by the FDA

MEXICAN STYLE QUINOA SALAD

Where it was distributed

MA, NH, NY, ME, VT

MassachusettsMaineNew HampshireNew YorkVermont

Questions about this recall

Why was it recalled?

contains undeclared soy and egg

Which lots are affected?

USE BY 1/22/24 UPC Codes: 0 36217 17201 8

Where was it sold?

MA, NH, NY, ME, VT

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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