CLASS I Food recall · Reported 16 Jun 2021 · FDA Enforcement Report

Hy-Vee Chicken Street taco kit recalled by Hy-Vee Stores

Hy-Vee Stores is recalling Hy-Vee Chicken Street taco kit, distributed in 8 states. The recall was initiated on 24 May 2021 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesUse by prior to May 27, 2021.
Quantity recalledunknown

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-0664-2021
FDA event ID
87991
Recalling firm
Hy-Vee Stores, West des Moines, IA
Brand
Hy-Vee
Classification
Class I
Status
Terminated
Recall initiated
24 May 2021
FDA classified
10 Jun 2021
Reported
16 Jun 2021
Type
Voluntary: Firm initiated
Customers notified by
Other
Reason category
Undeclared Egg
Product category
Ready Meals

Timeline

24 May 2021Recall initiated by company
10 Jun 2021Classified by FDA+17 days
16 Jun 2021Published in enforcement report+6 days

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

Reason for recall

Product contains chipotle crema as part of a taco kit which contains undeclared major food allergen egg

Product as listed by the FDA

Hy-Vee Chicken Street taco kit, Net Wt. 18 OZ, UPC 282503 212993.

Where it was distributed

Distributed to Hy-Vee grocery stores in IA, IL, KS, MN, MO, NE, SD, WI.

IowaIllinoisKansasMinnesotaMissouriNebraskaSouth DakotaWisconsin

Stores named: Hy-Vee, Chipotle

Questions about this recall

Why was it recalled?

Product contains chipotle crema as part of a taco kit which contains undeclared major food allergen egg

Which lots are affected?

Use by prior to May 27, 2021.

Where was it sold?

Distributed to Hy-Vee grocery stores in IA, IL, KS, MN, MO, NE, SD, WI.

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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