Frobright Salsary, LLC Recall: Salsa products are recalled due to potential contamination with wood particles.

🇺🇸 United States

1. April 17, 2025 - Recall initiated
2. May 28, 2025 - Reported by source
3. May 28, 2025 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0814-2025

Event ID

96829

Status

Terminated

Classification

Class II

Company

Frobright Salsary, LLC

Product description

Mild Salsa is refrigerated product, packaged in Polypropylene container, net wt. 14oz, UPC 1 18738 54632. San Juan Salsa Co. Arlington, WA 98223, www.sanjuansalsa.com

Quantity

Total 5839/14oz. containers and 1380 cases (12ct)

Reason

Salsa products are recalled due to potential contamination with wood particles.

Recall initiation date

April 17, 2025

Report date

May 28, 2025

Classification date

Not published in this source record

Termination date

May 28, 2025

Distribution pattern

Distributed in AK, ID, OR, and WA.

UPC, lot, and code information

Best Before Dates for San Juan Salsa: Mar 3 2025 Mar 7 2025 Mar 13 2025 Mar 19 2025 Mar 24 2025 Mar 26 2025 Mar 31 2025 Apr 7 2025 Apr 8 2025 Apr 15 2025 Apr 23 2025 Apr 25 2025 Apr 28 2025 May 1 2025 May 5 2025 May 7 2025 May 13 2025 May 20 2025 May 23 2025

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Other products recalled under this same event

This recall shares FDA event ID 96829 with 7 other product entries in Public Health Trace.

Responsible company: Frobright Salsary, LLC

Other recalls from Frobright Salsary, LLC

A map highlighting the states named in the source's distribution description.

Distributed No data published

Shading reflects state-level totals only, as published by the source. It does not imply county-level or point-level precision.

Distribution map

State	Distributed
Alaska	1
Idaho	1
Oregon	1
Washington	1

States shown are extracted from the source's free-text distribution description above; a narrative description (e.g. "distributed nationwide") may not list individual states to extract.

Where this information comes from

View FDA enforcement record -- the specific openFDA record this summary was built from.

No separate FDA public notice was found for this enforcement record. The information below comes from FDA's Recall Enterprise System through openFDA.

FDA Enforcement Reports -- FDA's general, official recall and enforcement information.

Technical source data

View raw source data -- the machine-readable record this page's information was built from.

Retrieved by Public Health Trace: July 18, 2026 ET

Frequently asked questions

What does a Class II mean?

A situation in which use of or exposure to a product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote.

Is this recall still active?

According to FDA, this recall's status is "Terminated." Always confirm the current status using the source links below, since status can change after Public Health Trace last retrieved this record.

What should I do if I have this product?

Follow the instructions published by the responsible agency (see the source links below) -- recall guidance (e.g. dispose of the product, return it for a refund, or check for a specific lot number) varies by recall and is set by that agency, not by Public Health Trace.

Where can I find more official information?

The source links below, published by FDA, are the authoritative record for this recall, including any updates issued after this summary was retrieved.

This summary is based on the official source record referenced above. Public Health Trace does not state that any company or product is unsafe beyond what the official source has published. Read the full medical disclaimer.

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