Oregon Nut Blend, Item # 5180808, Packed in cardboard box with poly liner; net wt. 25 lbs. No UPC. Label declares: Oreg
Summary
The FDA issued a Class I for Oregon Nut Blend, Item # 5180808, Packed in cardboard box with poly liner; net w by Willamette Hazelnut, Inc.. Reason: Undeclared Almonds and Cashews.
Details
Source
Food Recall
External ID
F-0892-2023
Action Date
2023-05-24
Status
Terminated
Category
food
Product Description
Oregon Nut Blend, Item # 5180808, Packed in cardboard box with poly liner; net wt. 25 lbs. No UPC. Label declares: Oregon Nut Blend, Innovative Bakery Resources. Ingredients: Hazelnuts, Walnuts. Product of USA. Manufactured By: Ardent Mills Tualatin, OR.
Lot/Code Info: Lot Code Production Date Expiration date 112200 3/7/2022 3/7/2023 112245 3/8/2022 3/8/2023 115908 6/24/2022 6/24/2023 116493 7/26/2022 7/26/2023 116863 9/16/2022 9/16/2023 116836 8/30/2022 8/30/2023 116876 9/16/2022 9/16/2023 116884 9/21/2022 9/21/2023 116889 9/21/2022 9/21/2023 200026 10/4/2022 10/4/2023 200286 11/7/2022 11/7/2023 200376 11/12/2022 11/12/2023 201247 1/18/2023 1/18/2024
Quantity Affected: 96,000 lbs
Reason for Recall
Undeclared Almonds and Cashews
Distribution
Distributed in OR
Type: Voluntary: Firm initiated
Recall Initiated: 2023-04-13
Company
Newberg, OR
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 74 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Willamette Hazelnut, Inc. has 2 FDA actions in our database, including 2 recalls.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (Willamette Hazelnut, Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Willamette Hazelnut, Inc. have FDA actions?
Willamette Hazelnut, Inc. has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0892-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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