Traditional Salsa is refrigerated product, packaged in Polypropylene container, net wt. 14oz, UPC 1 18738 54636. San Jua
Summary
The FDA issued a Class II for Traditional Salsa is refrigerated product, packaged in Polypropylene container, by Frobright Salsary, LLC. Reason: Salsa products are recalled due to potential contamination with wood particles..
Details
Source
Food Recall
External ID
F-0817-2025
Action Date
2025-05-28
Status
Terminated
Category
food
Product Description
Traditional Salsa is refrigerated product, packaged in Polypropylene container, net wt. 14oz, UPC 1 18738 54636. San Juan Salsa Co. Arlington, WA 98223, www.sanjuansalsa.com
Lot/Code Info: Best Before Dates for San Juan Salsa: Jan 29 2025 Feb 2 2025 Feb 5 2025 Feb 9 2025 Feb 12 2025 Feb 16 2025 Feb 19 2025 Feb 23 2025 Feb 24 2025 Feb 26 2025 Mar 5 2025 Mar 12 2025 Mar 17 2025 Mar 18 2025 Mar 26 2025 Mar 29 2025 Apr 2 2025 Apr 8 2025 Apr 12 2025 Apr 14 2025 Apr 16 2025 Apr 23 2025
Quantity Affected: 5143/14oz containers and 1572 cases (12ct)
Reason for Recall
Salsa products are recalled due to potential contamination with wood particles.
Distribution
Distributed in AK, ID, OR, and WA.
Type: Voluntary: Firm initiated
Recall Initiated: 2025-04-17
Company
Arlington, 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 56 food recalls issued in the same week, part of 204 food-related FDA actions this month.
Frobright Salsary, LLC has 8 FDA actions in our database, including 8 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 (Frobright Salsary, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Frobright Salsary, LLC have FDA actions?
Frobright Salsary, LLC has 8 FDA actions in our database, including 8 recalls and 0 device clearances.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "F-0817-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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