Class IITerminated in FDA datasetRecall initiated May 22, 2017

Ravioli Spinach. Product is made refrigerated. Product is packaged in plastic containers. The…

Recalling firm: Alaska Pasta Company

Why it was recalled

Undeclared soy lecithin. The firm used Canola oil cooking spray, which contains soy lecithin, in the manufacture of product but soy or soy lecithin is not declared on finished…

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: Oct 19, 2017.

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

ProductRavioli Spinach. Product is made refrigerated. Product is packaged in plastic containers. The plastic containers are marked on the side of the container with the customer name (middle top), date of production (bottom left), and weight of product in lbs (bottom right). Some containers have Alaska Pasta written on them. Product is not packaged for retail and weights vary depending on orders.

FDA code information

No lot codes. The date of production is marked on the side of the plastic container.

Match the product, package size, and code together. A missing match does not guarantee safety.

Full FDA record and distribution details

Original product description

Ravioli Spinach. Product is made refrigerated. Product is packaged in plastic containers. The plastic containers are marked on the side of the container with the customer name (middle top), date of production (bottom left), and weight of product in lbs (bottom right). Some containers have Alaska Pasta written on them. Product is not packaged for retail and weights vary depending on orders.

Original FDA recall reason

Undeclared soy lecithin. The firm used Canola oil cooking spray, which contains soy lecithin, in the manufacture of product but soy or soy lecithin is not declared on finished product label.

Recall details

Recall number
F-2352-2017
Event ID
77356
FDA status
Terminated
Initiated
May 22, 2017
Reported
Jun 14, 2017
Classified
Jun 7, 2017
Terminated
Oct 19, 2017
Quantity
18.90 lbs.
Location
Anchorage, AK, United States
Initiation type
Voluntary: Firm initiated
Notification
Visit

Where it was distributed

distributed in AK only.

FDA source record · F-2352-2017

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

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