CLASS III Food recall · Reported 12 May 2021 · FDA Enforcement Report

Thai Home Sweet Chili Paste (Num Prik Pao) recalled by Jansala & Foods

Jansala & Foods is recalling Thai Home Sweet Chili Paste (Num Prik Pao), distributed in California, Oregon, Washington. The recall was initiated on 23 Apr 2021 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesAll Best-by dates through March 2022.
Quantity recalled265 cases (3180 jars)

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

Recall details

Recall number
F-0474-2021
FDA event ID
87805
Recalling firm
Jansala & Foods, Portland, OR
Classification
Class III
Status
Terminated
Recall initiated
23 Apr 2021
FDA classified
4 May 2021
Reported
12 May 2021
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Foreign Material
Product category
Other

Timeline

23 Apr 2021Recall initiated by company
4 May 2021Classified by FDA+11 days
12 May 2021Published in enforcement report+8 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

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

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

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 [email protected] Distributed by: Earthly Gourmet 2143 SE Lafayette St Portland, OR 97202 [email protected] 503-853-3110 The label also states, Vegan No MSG Added No artificial fillers or flavour enhancers

Where it was distributed

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

CaliforniaOregonWashington

Questions about this recall

Why was it recalled?

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

Which lots are affected?

All Best-by dates through March 2022.

Where was it sold?

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

What should I do if I have it?

Do not eat it. Return it to the store for a refund or throw it away. If you have symptoms after eating it, contact a doctor.

What does Class III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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