Orzo (vegan) Dried, net wt. 10oz in clear package with green/back printings on white label. UPC 810135110747.
Summary
The FDA issued a Class II for Orzo (vegan) Dried, net wt. 10oz in clear package with green/back printings on w by PASTAURORA LLC. Reason: Product is recalled due to potential mold growth contamination..
Details
Source
Food Recall
External ID
F-1517-2024
Action Date
2024-08-07
Status
Terminated
Category
food
Product Description
Orzo (vegan) Dried, net wt. 10oz in clear package with green/back printings on white label. UPC 810135110747.
Lot/Code Info: Lot WBF-SEMPLV-CL-050724-A and the expiration date of May 7, 2025. Breakdown of code: Company abbreviation-dough formulation-location-date-batch.
Quantity Affected: 27 packages
Reason for Recall
Product is recalled due to potential mold growth contamination.
Distribution
Distributed in WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2024-06-24
Company
Clinton, WA
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 105 food recalls issued in the same week, part of 204 food-related FDA actions this month.
PASTAURORA LLC has 2 FDA actions in our database, including 2 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 (PASTAURORA LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does PASTAURORA LLC have FDA actions?
PASTAURORA LLC has 2 FDA actions in our database, including 2 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-1517-2024" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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