Hy-Vee Stores Inc Recall: Product contained an ingredient that tested positive for Salmonella.

🇺🇸 United States

1. January 4, 2019 - Recall initiated
2. February 13, 2019 - Reported by source
3. February 11, 2019 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0830-2019

Event ID

81904

Status

Terminated

Classification

Class I

Company

Hy-Vee Stores Inc

Product description

HyVee brand Salted Caramel-flavored Bettercreme cheese cakes packaged in the following ways: 1) Sea Salted Caramel Bettercreme Cheesecake, Net Wt. 7 OZ, HyVee West Des Moines, IA UPC 02 82325 XXXXX packaged in clear plastic containers; 2) Sea Salted Caramel Bettercreme Cheesecake, Net Wt. 27 OZ, HyVee West Des Moines, IA 02 82326 XXXXX, packaged in clear plastic containers;

Quantity

2,608 32 oz and other similar sizes; 4,367 8 oz and other similar sizes

Reason

Product contained an ingredient that tested positive for Salmonella.

Recall initiation date

January 4, 2019

Report date

February 13, 2019

Classification date

Not published in this source record

Termination date

February 11, 2019

Distribution pattern

Distributed to consumers in Iowa, Illinois, Missouri, Kansas, Nebraska, South Dakota, Minnesota and Wisconsin.

UPC, lot, and code information

Expiration date range between December 6, 2018 and January 11, 2019

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Press Release

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 81904 with 9 other product entries in Public Health Trace.

Responsible company: Hy-Vee Stores Inc

Other recalls from Hy-Vee Stores Inc

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: July 18, 2026 ET

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.

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