The Toasted Oat Recall: Ingredient containing mold was used in production

🇺🇸 United States

1. March 15, 2021 - Recall initiated
2. April 14, 2021 - Reported by source
3. March 15, 2023 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0430-2021

Event ID

87516

Status

Terminated

Classification

Class II

Company

The Toasted Oat

Product description

The Toasted Oat Bakehouse Blueberry Cobbler Soft Granola (6 -10 oz pouches per case); and Soft Granola Crumble Bars Blueberry Cobbler (5 - 28.3g bars per pack/6 packs per case)

Quantity

145,000 (total of 28.3g bars); 87905 (total of 10oz Pouches)

Reason

Ingredient containing mold was used in production

Recall initiation date

March 15, 2021

Report date

April 14, 2021

Classification date

Not published in this source record

Termination date

March 15, 2023

Distribution pattern

Distributed to all US States with the exception of North and South Dakota

UPC, lot, and code information

Batch No - MSA23, MSA24 Lot No - 600079, 700079, 800079, 900079, 600080, 700080, 900080 UPC for 10oz Pouches : 860459000163, 860459000170, 860459000187, 860459000194; UPC for 28.3g Bars : 86000820042, 86000820066, 860000820080 Best By 10/24/21 for lots ending in 00079 Best By 12/03/21 for lots ending in 00080

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

Other products recalled under this same event

This recall shares FDA event ID 87516 with 3 other product entries in Public Health Trace.

Responsible company: The Toasted Oat

Other recalls from The Toasted Oat

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 II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

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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