CV EAST LLC, CORNERSTONE MARION LLC Recall: Caf¿ Valley Inc. of Marion, Indiana is voluntarily recalling cases of Banana nut mini muffins labeled as Lemon poppy seed mini muffins, because they may contain undeclared allergen walnuts.

🇺🇸 United States

1. September 16, 2016 - Recall initiated
2. November 30, 2016 - Reported by source
3. February 13, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0481-2017

Event ID

75294

Status

Terminated

Classification

Class I

Company

CV EAST LLC, CORNERSTONE MARION LLC

Product description

12ct Banana Nut mini muffins labeled as 12ct Lemon poppy seed mini muffins; Date code 160803 ink jet printed on top near the label.

Quantity

1170 cases of Banana nut mini muffins labeled as Lemon poppy seed mini muffins

Reason

Caf¿ Valley Inc. of Marion, Indiana is voluntarily recalling cases of Banana nut mini muffins labeled as Lemon poppy seed mini muffins, because they may contain undeclared allergen walnuts.

Recall initiation date

September 16, 2016

Report date

November 30, 2016

Classification date

Not published in this source record

Termination date

February 13, 2017

Distribution pattern

Domestic: Alabama, Illinois, Kansas, Massachusetts, Mississippi, Missouri, Ohio, Vermont.

UPC, lot, and code information

Date code 160803 ink jet printed on top near the label; #71205 12ct Banana Nut Muffin; MFM 08/03/16 time BEST BY 05/03/17; GTIN code: 10040697712050, UPC: 0 40697 71213 8

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

E-Mail

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: CV EAST LLC, CORNERSTONE MARION LLC

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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