Class IITerminated in FDA datasetRecall initiated May 5, 2023

Multigrain Spicy Salmon Avocado Roll, net wt. 7 oz., Ready to Eat, perishable and refrigerated…

Recalling firm: Origami Catering, LLC

Why it was recalled

The ingredients statement declares Sesame but the Contains statement does not declare sesame. Sesame seeds are visible on product.

Historical recall record. This is not a new recall announcement. “Terminated” describes the FDA recall process; it does not certify that an individual package is safe. FDA termination date: Jun 13, 2023.

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Compare the exact product and package details with the label you have.

ProductMultigrain Spicy Salmon Avocado Roll, net wt. 7 oz., Ready to Eat, perishable and refrigerated product. UPC 8 51016 00244 7. Manufactured by Origami Catering 828 N Killingsworth St., Portland, OR 97217. The Ingredients statement is read in part: Multigrain Sushi Rice ***, Salmon (fish), Avocado, ***Mayonnaise (egg)***Sriracha***Toasted Sesame Seeds***Allergen: Contains Fish (salmon), Egg.
Package size7 oz
UPC851016002447

FDA code information

Made on 5/4/23 Best Before 5/6/23 Made on 5/5/23 Best Before 5/7/23

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Full FDA record and distribution details

Original product description

Multigrain Spicy Salmon Avocado Roll, net wt. 7 oz., Ready to Eat, perishable and refrigerated product. UPC 8 51016 00244 7. Manufactured by Origami Catering 828 N Killingsworth St., Portland, OR 97217. The Ingredients statement is read in part: Multigrain Sushi Rice ***, Salmon (fish), Avocado, ***Mayonnaise (egg)***Sriracha***Toasted Sesame Seeds***Allergen: Contains Fish (salmon), Egg.

Extracted codes and context

TypeCode / valueContext
UPC851016002447ado Roll, net wt. 7 oz., Ready to Eat, perishable and refrigerated product. UPC 8 51016 00244 7. Manufactured by Origami Catering 828 N Killingsworth St., Portland, OR 97217. The Ingredients statement is read in pa

Original FDA recall reason

The ingredients statement declares Sesame but the Contains statement does not declare sesame. Sesame seeds are visible on product.

Recall details

Recall number
F-0965-2023
Event ID
92291
FDA status
Terminated
Initiated
May 5, 2023
Reported
Jun 7, 2023
Classified
May 30, 2023
Terminated
Jun 13, 2023
Quantity
89 packages
Location
Portland, OR, United States
Initiation type
Voluntary: Firm initiated
Notification
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Where it was distributed

distributed in Oregon and Washington

FDA source record · F-0965-2023

Data updated September 16, 2026. View official FDA data ↗

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