CLASS II Food recall · Reported 20 Mar 2019 · FDA Enforcement Report

Joy Green Chilli Chutney recalled by Joy Gourmet Foods

Joy Gourmet Foods is recalling Joy Green Chilli Chutney, distributed in Connecticut, New Jersey, New York. The recall was initiated on 25 Feb 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes0522, 0906 5/22/2019, 9/6/2019
Quantity recalledunknown

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-1222-2019
FDA event ID
82250
Recalling firm
Joy Gourmet Foods, Maspeth, NY
Brand
Joy
Classification
Class II
Status
Terminated
Recall initiated
25 Feb 2019
FDA classified
29 Mar 2019
Reported
20 Mar 2019
Type
Voluntary: Firm initiated
Customers notified by
Visit
Reason category
Undeclared Sulfites
Product category
Other

Timeline

25 Feb 2019Recall initiated by company
20 Mar 2019Published in enforcement report+23 days
29 Mar 2019Classified by FDA+9 days

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

Reason for recall

Product contains undeclared sulfites.

Product as listed by the FDA

JOY GREEN CHILLI CHUTNEY NET WT 8 OZ (228g), UPC: 6 80617 60412 1

Where it was distributed

CT, NY, NJ

ConnecticutNew JerseyNew York

Questions about this recall

Is Joy Green Chilli Chutney recalled?

Yes. Joy Gourmet Foods recalled Joy Green Chilli Chutney on 25 Feb 2019. The recall is Class II and its status is Terminated. Recall number F-1222-2019.

Why was it recalled?

Product contains undeclared sulfites.

Which lots are affected?

0522, 0906 5/22/2019, 9/6/2019

Where was it sold?

CT, NY, NJ

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 II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 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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