Michele's Granola LLC Recall: Michele's Granola LLC. has initiated a recall of MOM s Salted Maple Pecan Granola, because of incorrectly labelled bags. (The incorrect back label with ingredient list does not list pecans as an ingredient.) Lot Number: 8/14/2020 , Best By date: 8/14/2020 . - F-0786-2020

🇺🇸 United States

1. February 21, 2020 - Recall initiated
2. March 11, 2020 - Reported by source
3. July 13, 2020 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0786-2020

Event ID

85058

Status

Terminated

Classification

Class II

Company

Michele's Granola LLC

Product description

Michele s Granola, MOM s Salted Maple Pecan Granola, 4 Cases of 12-12 oz. stand up pouches.

Quantity

4 cases of 12-12oz bags were made and distributed.

Reason

Michele's Granola LLC. has initiated a recall of MOM s Salted Maple Pecan Granola, because of incorrectly labelled bags. (The incorrect back label with ingredient list does not list pecans as an ingredient.) Lot Number: 8/14/2020 , Best By date: 8/14/2020 .

Recall initiation date

February 21, 2020

Report date

March 11, 2020

Classification date

Not published in this source record

Termination date

July 13, 2020

Distribution pattern

The product was distributed to one retail chain in the following locations: Maryland and Washington D. C.

UPC, lot, and code information

Lot Number: 8/14/2020 Best By date: 8/14/2020

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Telephone

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: Michele's Granola LLC

Other recalls from Michele's Granola LLC

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 II mean?

FDA classifies this recall as Class II. 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 July 13, 2020.

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.

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