Whole Foods Market Brand 365, Llc Recall: According to the firm, packaged crusts used in various tarts these tarts contains Almond Flour (Nuts) which is listed as an ingredient on the package, but is not listed as an ingredient on the WFM scale label.

🇺🇸 United States

1. January 2, 2017 - Recall initiated
2. February 22, 2017 - Reported by source
3. July 5, 2017 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-1472-2017

Event ID

76157

Status

Terminated

Classification

Class I

Company

Whole Foods Market Brand 365, Llc

Product description

Whole Foods Market, TART KEY LIME 4IN TART KEY LIME 4IN,TART KEY LIME 9IN

Quantity

4822

Reason

According to the firm, packaged crusts used in various tarts these tarts contains Almond Flour (Nuts) which is listed as an ingredient on the package, but is not listed as an ingredient on the WFM scale label.

Recall initiation date

January 2, 2017

Report date

February 22, 2017

Classification date

Not published in this source record

Termination date

July 5, 2017

Distribution pattern

According to the firm the product was distributed in New Jersey, Pennsylvania, Maryland, Virginia, District of Columbia, Ohio, Kentucky.

UPC, lot, and code information

24989600000 TART KEY LIME 4IN 23144500000 TART KEY LIME 4IN 24988900000 TART KEY LIME 9IN

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 76157 with 7 other product entries in Public Health Trace.

Responsible company: Whole Foods Market Brand 365, Llc

Other recalls from Whole Foods Market Brand 365, 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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