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Garden Of Light Inc. Recall: Product labeled containing pecans actually contains almonds

United States

TerminatedClass II

Company
Garden Of Light Inc.
Product
(a) SEVEN SUNDAYS VANILLA CHERRY PECAN MUESLI 12oz. pouch,…
Recall date
August 14, 2017
Terminated
August 16, 2018
Source
FDA

Reason for recall

Product labeled containing pecans actually contains almonds

  1. - Recall initiated
  2. - Reported by source
  3. - Recall terminated
Recalled products
Product description UPC Quantity Lot / code information
(a) SEVEN SUNDAYS VANILLA CHERRY PECAN MUESLI 12oz. pouch, UPC: 8-56088-00315-6 (b) SEVEN SUNDAYS VANILLA CHERRY PECAN MUESLI 2oz. cup UPC: 8-56088-00311-8 8-56088-00315-6 (a) 1098 cases (b) 20 cases a)LOT CODES: JUNE 29,2018 & AUGUST 11,2018 (b) LOT CODES: AUGUST 11, 2018

Distribution

  • Nationwide

Official source record

Agency
FDA
Dataset
FDA Food Enforcement (Recalls)
Recall number
F-3470-2017
Event ID
77947
Status
Terminated
Classification
Class II
Company
Garden Of Light Inc.
Product description
(a) SEVEN SUNDAYS VANILLA CHERRY PECAN MUESLI 12oz. pouch, UPC: 8-56088-00315-6 (b) SEVEN SUNDAYS VANILLA CHERRY PECAN MUESLI 2oz. cup UPC: 8-56088-00311-8
Quantity
(a) 1098 cases (b) 20 cases
Reason
Product labeled containing pecans actually contains almonds
Recall initiation date
August 14, 2017
Report date
September 6, 2017
Classification date
Not published in this source record
Termination date
August 16, 2018
Distribution pattern
Nationwide
UPC, lot, and code information
UPC 8-56088-00315-6; a)LOT CODES: JUNE 29,2018 & AUGUST 11,2018 (b) LOT CODES: AUGUST 11, 2018
Voluntary or mandated
Voluntary: Firm initiated
Initial notification method
Letter
Source last updated
Not tracked separately from the Public Health Trace retrieval date below
Public Health Trace retrieval date

Responsible company: Garden Of Light Inc.

Other recalls from Garden Of Light Inc.

FDA Recall United States Terminated Historical recordClass I

Garden Of Light Inc.

Product
WOODSTOCK ORGANIC MATCHA VANILLA OATS, 1.8 oz (50g) cup UPC…
Published
August 16, 2017
Distribution
Nationwide

View recall →

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 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.