BDAY CAKE MOCHI CRUNCH packed in pink plastic pouch packaging, net wt. 5oz, UPC 7189147148, Orwaiian LLC, 465 NE Burnsid
Summary
The FDA issued a Class II for BDAY CAKE MOCHI CRUNCH packed in pink plastic pouch packaging, net wt. 5oz, UPC by Orwaiian LLC. Reason: Label has a Contains statement that is missing milk and coconut (tree nut) that are declared in the ingredients statement..
Details
Source
Food Recall
External ID
F-1800-2024
Action Date
2024-09-18
Status
Terminated
Category
food
Product Description
BDAY CAKE MOCHI CRUNCH packed in pink plastic pouch packaging, net wt. 5oz, UPC 7189147148, Orwaiian LLC, 465 NE Burnside Rd Gresham, OR 97030. The label declares "***Ingredients: Sesame Seeds, Milk Powder, Nonfat dry milk, Soy Lecithin, Coconut ***CONTAINS: Soy, Sesame ***MANUFACTURED in a facility that also processes: MILK ***SOY, SESAME***COCONUT***".
Lot/Code Info: MFG Code: MCBD05. Expiry dates of 07-29-2025 or earlier. MFG Code breakdown as Mochi Crunch B Day 5oz
Quantity Affected: 720 units
Reason for Recall
Label has a Contains statement that is missing milk and coconut (tree nut) that are declared in the ingredients statement.
Distribution
Product distributed in CA, HI, OR, WA, and Washington DC.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-08-21
Company
Gresham, OR
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 43 food recalls issued in the same week, part of 204 food-related FDA actions this month.
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 (Orwaiian LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Orwaiian LLC have FDA actions?
This is the only FDA action we have on record for Orwaiian LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1800-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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