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Whole Foods Market Brand 365, Llc Recall: Undeclared (peanut) allergen: 365 Organic Peanut Butter and Cocoa Balls were packaged into 365 Organic Raisin Bran Flakes boxes.

United States

TerminatedClass I

Company
Whole Foods Market Brand 365, Llc
Product
365 Organic Raisin Bran Flakes 15 oz. packaged in plastic ba…
Recall date
October 6, 2017
Terminated
January 4, 2018
Source
FDA

Reason for recall

Undeclared (peanut) allergen: 365 Organic Peanut Butter and Cocoa Balls were packaged into 365 Organic Raisin Bran Flakes boxes.

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
365 Organic Raisin Bran Flakes 15 oz. packaged in plastic bag, then cardboard box Not published in this source record 875 cases (10500 units) distributed Best If Used By June 04 18

Distribution

  • Nationwide throughout the US and via amazon.com

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-0036-2018
Event ID
78238
Status
Terminated
Classification
Class I
Company
Whole Foods Market Brand 365, Llc
Product description
365 Organic Raisin Bran Flakes 15 oz. packaged in plastic bag, then cardboard box
Quantity
875 cases (10500 units) distributed
Reason
Undeclared (peanut) allergen: 365 Organic Peanut Butter and Cocoa Balls were packaged into 365 Organic Raisin Bran Flakes boxes.
Recall initiation date
October 6, 2017
Report date
November 1, 2017
Classification date
Not published in this source record
Termination date
January 4, 2018
Distribution pattern
Nationwide throughout the US and via amazon.com
UPC, lot, and code information
Best If Used By June 04 18
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Press Release
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Whole Foods Market Brand 365, Llc

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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:

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?

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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.