Medium Salsa is refrigerated product, packaged in Polypropylene container, net wt. 14oz, UPC 1 18738 54633. San Juan Sal
Summary
The FDA issued a Class II for Medium Salsa is refrigerated product, packaged in Polypropylene container, net w by Frobright Salsary, LLC. Reason: Salsa products are recalled due to potential contamination with wood particles..
Details
Source
Food Recall
External ID
F-0815-2025
Action Date
2025-05-28
Status
Terminated
Category
food
Product Description
Medium Salsa is refrigerated product, packaged in Polypropylene container, net wt. 14oz, UPC 1 18738 54633. San Juan Salsa Co. Arlington, WA 98223, www.sanjuansalsa.com
Lot/Code Info: Best Before Dates for San Juan Salsa: Feb 27 2025 Feb 28 2025 Mar 1 2025 Mar 4 2025 Mar 10 2025 Mar 11 2025 Mar 14 2025 Mar 17 2025 Mar 17 2025 Mar 18 2025 Mar 19 2025 Mar 20 2025 Mar 21 2025 Mar 24 2025 Mar 25 2025 Mar 26 2025 Mar 27 2025 Mar 28 2025 Mar 31 2025 Apr 1 2025 Apr 2 2025 Apr 3 2025 Apr 4 2025 Apr 8 2025 Apr 9 2025 Apr 10 2025 Apr 11 2025 Apr 15 2025 Apr 16 2025 Apr 17 2025 Apr 21 2025 Apr 22 2025 Apr 23 2025 Apr 24 2025 Apr 28 2025 Apr 29 2025 Apr 30 2025 May 1 2025 May 5 2025 May 6 2025 May 8 2025 May 12 2025 May 13 2025 May 14 2025 May 15 2025 May 16 2025 May 19 2025 May 20 2025 May 21 2025 May 22 2025
Quantity Affected: 27514/14 oz. containers and 2424 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-0815-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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