Check the Batch
Class IITerminated in FDA datasetRecall initiated Sep 2, 2014

Tullia's Italian Meatless Pasta Sauce, packaged in a 16 oz. (436g) and 32 oz. (872g) glass jars…

Recalling firm: Tullia's

Why it was recalled

Italian Meatless Pasta Sauce is recalled because review of the production records revealed that one batch of sauce produced had a pH high enough to allow the growth of Clostridium…

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: Feb 13, 2015.

Check your package

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

ProductTullia's Italian Meatless Pasta Sauce, packaged in a 16 oz. (436g) and 32 oz. (872g) glass jars with one-piece metal closures. The 32 oz. (872g) glass jar has the UPC 7 48863 64322 3. The 16 oz (436g) glass jar has the UPC 7 48863 64321 6.
Package size16 oz
UPC748863643216, 748863643223

FDA code information

Code 530140

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

Full FDA record and distribution details

Original product description

Tullia's Italian Meatless Pasta Sauce, packaged in a 16 oz. (436g) and 32 oz. (872g) glass jars with one-piece metal closures. The 32 oz. (872g) glass jar has the UPC 7 48863 64322 3. The 16 oz (436g) glass jar has the UPC 7 48863 64321 6.

Extracted codes and context

TypeCode / valueContext
UPC748863643216glass jar has the UPC 7 48863 64322 3. The 16 oz (436g) glass jar has the UPC 7 48863 64321 6.
UPC748863643223jars with one-piece metal closures. The 32 oz. (872g) glass jar has the UPC 7 48863 64322 3. The 16 oz (436g) glass jar has the UPC 7 48863 64321 6.

Original FDA recall reason

Italian Meatless Pasta Sauce is recalled because review of the production records revealed that one batch of sauce produced had a pH high enough to allow the growth of Clostridium botulinum, a bacterium which can cause life-threatening illness or death.

Recall details

Recall number
F-0024-2015
Event ID
69168
FDA status
Terminated
Initiated
Sep 2, 2014
Reported
Oct 22, 2014
Classified
Oct 10, 2014
Terminated
Feb 13, 2015
Quantity
312 jars (16 oz. each) and 172 jars (32 oz. each)
Location
Spokane, WA, 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 Spokane area of Washington.

FDA source record · F-0024-2015

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

Follow official FDA and manufacturer guidance.