Dawn Food Products Inc. Recall: Products may contain Salmonella. These products contain ingredients recalled by Valley Milk Products for potential Salmonella contamination. - F-1990-2017

🇺🇸 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-1990-2017

Event ID

75991

Status

Terminated

Classification

Class I

Company

Dawn Food Products Inc.

Product description

R&H VANILLA Speedy Creme Instant Pudding and Pie Filling Mix Item 00727521 4 lbs 2 oz retail paper bag, six retail bags per case

Quantity

427 cases

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: 61417130 61417131 61587135 61587136 61657130 61657130 62327131 62327132 62567101 62567102 62567103 62567104 62817131 62817132

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.

This record comes from FDA's Enforcement Report database. Not every Enforcement Report record has a separate FDA.gov recall-announcement page.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information. See FDA Enforcement Reports versus recall announcements for how that database differs from a press-release-style announcement.

New to reading a recall record? See how to read an FDA recall record and what recall statuses mean.

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?

FDA classifies this recall as Class I. See how to read an FDA recall record (linked above) for what each classification level means.

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 responsible agency's published instructions, linked below -- recall guidance is set by that agency, not by Public Health Trace.

Official guidance and record verification

Public Health Trace does not provide medical advice -- review the linked official source below for current, authoritative information.

How to interpret this historical record

This record is preserved as published by FDA, as of September 28, 2017.

Status as reported: Terminated.

This page does not imply a current danger or a current consumer instruction -- review the official source for the most current information.

View the official FDA source

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.

• Email
• X / Twitter
• Facebook