RecallHawk
Class II Recall

Verde Salsa is refrigerated product, packaged in Polypropylene container, net wt. 12.5 oz, UPC 1 18738 03719. San Juan S

Frobright Salsary, LLC

Summary

The FDA issued a Class II for Verde Salsa is refrigerated product, packaged in Polypropylene container, net wt by Frobright Salsary, LLC. Reason: Salsa products are recalled due to potential contamination with wood particles..

Details

Source

Food Recall

External ID

F-0820-2025

Action Date

2025-05-28

Status

Terminated

Category

food

Product Description

Verde Salsa is refrigerated product, packaged in Polypropylene container, net wt. 12.5 oz, UPC 1 18738 03719. San Juan Salsa Co. Arlington, WA 98223, www.sanjuansalsa.com

Lot/Code Info: Best Before Dates for San Juan Salsa: Jan 21 2025 Jan 31 2025 Feb 9 2025 Feb 18 2025 Feb 25 2025 Mar 7 2025 Mar 15 2025 Mar 25, 2025 Mar 31, 2025 Apr 4 2025 Apr 14 2025

Quantity Affected: 491/12.5 oz containers.

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

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-0820-2025" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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