Dawn Food Products Inc. Recall: Products may contain Salmonella. These products contain ingredients recalled by Valley Milk Products for potential Salmonella contamination.

🇺🇸 United States

1. December 9, 2016 - Recall initiated
2. April 26, 2017 - Reported by source
3. September 28, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1989-2017

Event ID

75991

Status

Terminated

Classification

Class I

Company

Dawn Food Products Inc.

Product description

QUIK 'N CREAMY VANILLA POWDERED FILLING Item number 00014100 25 pound bag

Quantity

3032 bags

Reason

Products may contain Salmonella. These products contain ingredients recalled by Valley Milk Products for potential Salmonella contamination.

Recall initiation date

December 9, 2016

Report date

April 26, 2017

Classification date

Not published in this source record

Termination date

September 28, 2017

Distribution pattern

Nationwide

UPC, lot, and code information

Lot: 61987101 61987102 61987103 61987104 61987105 61987106 61987107 62437101 62437102 62437103 62437104 62437105 62437106 62437107 62737102 62737103 62737104 62737105 62737106 62737107 62817123

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

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 75991 with 4 other product entries in Public Health Trace.

Responsible company: Dawn Food Products Inc.

Other recalls from Dawn Food Products 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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