Jansala & Foods LLC Recall: Failure to manufacture product in accordance with 21CFR part 114: Acidified Foods

🇺🇸 United States

1. April 23, 2021 - Recall initiated
2. May 12, 2021 - Reported by source
3. July 28, 2021 - Recall terminated

Official source record

Agency

FDA

Dataset

FDA Food Enforcement (Recalls)

Recall number

F-0474-2021

Event ID

87805

Status

Terminated

Classification

Class III

Company

Jansala & Foods LLC

Product description

Thai Home brand Sweet Chili Paste (Num Prik Pao) packaged in glass jars. Net weight 6.5 oz (180g). Refrigerate after opening. UPC 8616080004054 Manufactured by: Jansala & Foods LLC 1813 NE 2nd Avenue Portland, OR ansalafoods@gmail.com Distributed by: Earthly Gourmet 2143 SE Lafayette St Portland, OR 97202 info@earthlygourmet.com 503-853-3110 The label also states, Vegan No MSG Added No artificial fillers or flavour enhancers

Quantity

265 cases (3180 jars)

Reason

Failure to manufacture product in accordance with 21CFR part 114: Acidified Foods

Recall initiation date

April 23, 2021

Report date

May 12, 2021

Classification date

Not published in this source record

Termination date

July 28, 2021

Distribution pattern

The products were distributed by the firm's distributor to 55 retailers in CA, OR, and WA.

UPC, lot, and code information

UPC 8616080004054; All Best-by dates through March 2022.

Voluntary or mandated

Voluntary: Firm initiated

Initial notification method

Telephone

Source last updated

Not tracked separately from the Public Health Trace retrieval date below

Public Health Trace retrieval date

July 18, 2026 ET

Responsible company: Jansala & Foods LLC

Other recalls from Jansala & Foods 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
California	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 III mean?

A situation in which use of or exposure to a product is not likely to cause adverse health consequences.

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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