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Hy-Vee Stores Inc Recall: Product contains chipotle crema as part of a taco kit which contains undeclared major food allergen egg

United States

TerminatedClass I

Company
Hy-Vee Stores Inc
Product
Hy-Vee Chicken Street taco kit, Net Wt. 18 OZ, UPC 282503 2…
Recall date
May 24, 2021
Terminated
July 8, 2021
Source
FDA

Reason for recall

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

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
Hy-Vee Chicken Street taco kit, Net Wt. 18 OZ, UPC 282503 212993. 282503 unknown Use by prior to May 27, 2021.

Distribution

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

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0664-2021
Event ID
87991
Status
Terminated
Classification
Class I
Company
Hy-Vee Stores Inc
Product description
Hy-Vee Chicken Street taco kit, Net Wt. 18 OZ, UPC 282503 212993.
Quantity
unknown
Reason
Product contains chipotle crema as part of a taco kit which contains undeclared major food allergen egg
Recall initiation date
May 24, 2021
Report date
June 16, 2021
Classification date
Not published in this source record
Termination date
July 8, 2021
Distribution pattern
Distributed to Hy-Vee grocery stores in IA, IL, KS, MN, MO, NE, SD, WI.
UPC, lot, and code information
UPC 282503; Use by prior to May 27, 2021.
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Other
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Hy-Vee Stores Inc

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Distribution map

A map highlighting the states named in the source's distribution description.

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map
State Distributed
Iowa 1
Illinois 1
Kansas 1
Minnesota 1
Missouri 1
Nebraska 1
South Dakota 1
Wisconsin 1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace:

Frequently asked questions

What does a Class I mean?

A situation in which there is a reasonable probability that use of or exposure to a product will cause serious adverse health consequences or death.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.