Rabbit Creek Products Inc. Recall: Bread, muffin, and brownie mixes may have been manufactured with flour contaminated with E. coli O121

🇺🇸 United States

1. August 9, 2016 - Recall initiated
2. October 12, 2016 - Reported by source
3. January 10, 2018 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-2523-2016

Event ID

74890

Status

Terminated

Classification

Class I

Company

Rabbit Creek Products Inc.

Product description

Killer Mudd Brownie Mix, packaged in a plastic bag which is placed in a cardboard box, net wt. 12.25oz, UPC 010749011106 (Brand names: Rabbit Creek Products, Heart of Iowa Market Place, Soulard Spice Shop, The Farmers House, and The Woods)

Quantity

139 bags

Reason

Bread, muffin, and brownie mixes may have been manufactured with flour contaminated with E. coli O121

Recall initiation date

August 9, 2016

Report date

October 12, 2016

Classification date

Not published in this source record

Termination date

January 10, 2018

Distribution pattern

Distributed nationwide to specialty shops and some products were sold online through the firm's website as well as Amazon.

UPC, lot, and code information

UPC 010749011106; Rabbit Creek Products brand: best by Feb 2017 and March 2017 Heart of Iowa Market Place brand: best by March 2017 Soulard Spice Shop brand: best by Feb 2017 The Farmers House brand: best by March 2017 The Woods brand: best by March 2017

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 74890 with 10 other product entries in Public Health Trace.

Responsible company: Rabbit Creek Products Inc.

Other recalls from Rabbit Creek 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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