Woodstock 5 Grain Cereal. Oats, Rye, Triticale, Barley, Golden Flax. Net Wt. 18.5 oz (1 lb 2.5 oz) 524g. UPC 0 42563-
Summary
The FDA issued a Class II for Woodstock 5 Grain Cereal. Oats, Rye, Triticale, Barley, Golden Flax. Net Wt. 1 by UNFI General Corporate. Reason: The ingredient Triticale is not identified as wheat..
Details
Source
Food Recall
External ID
F-0872-2024
Action Date
2024-02-21
Status
Terminated
Category
food
Product Description
Woodstock 5 Grain Cereal. Oats, Rye, Triticale, Barley, Golden Flax. Net Wt. 18.5 oz (1 lb 2.5 oz) 524g. UPC 0 42563-01772 9. Distributed by Woodstock, 313 Iron Horse Way, Providence, RI 02908. Packaged in a plant that also processes wheat.
Lot/Code Info: Best By Dates: MAR0625, SEP1224, JUL1624, JUN2624
Quantity Affected: 73,872 canisters
Reason for Recall
The ingredient Triticale is not identified as wheat.
Distribution
Nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2024-01-18
Company
Providence, RI
Context & Analysis
This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.
This was one of 60 food recalls issued in the same week, part of 204 food-related FDA actions this month.
UNFI General Corporate has 31 FDA actions in our database, including 31 recalls.
Frequently Asked Questions
What is a Class II recall?
A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.
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 (UNFI General Corporate) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does UNFI General Corporate have FDA actions?
UNFI General Corporate has 31 FDA actions in our database, including 31 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0872-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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