CLASS II Food recall · Reported 1 Jul 2026 · FDA Enforcement Report

Joy Orange Lassi recalled by Joy Gourmet Foods

Joy Gourmet Foods is recalling Joy Orange Lassi, distributed in New Jersey, New York, Pennsylvania. The recall was initiated on 23 Apr 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesExpiry June 30 through July 30, 2026 UPC: 68061710033
Quantity recalled50 gallons (total)

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
H-1093-2026
FDA event ID
98975
Recalling firm
Joy Gourmet Foods, Maspeth, NY
Brand
Joy
Classification
Class II
Status
Completed
Recall initiated
23 Apr 2026
FDA classified
23 Jun 2026
Reported
1 Jul 2026
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Processing Deviation
Product category
Citrus

Timeline

23 Apr 2026Recall initiated by company
23 Jun 2026Classified by FDA+61 days
1 Jul 2026Published 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

Product not adequately pasteurized

The USDA issues these when meat or poultry was produced without proper inspection, or when a step such as cooking or pasteurisation did not meet requirements.

Product as listed by the FDA

Joy Orange Lassi 16 oz.

Where it was distributed

NY, NJ, PA

New JerseyNew YorkPennsylvania

Stores named: Walmart

Questions about this recall

Is Joy Orange Lassi recalled?

Yes. Joy Gourmet Foods recalled Joy Orange Lassi on 23 Apr 2026. The recall is Class II and its status is Completed. Recall number H-1093-2026.

Why was it recalled?

Product not adequately pasteurized

Which lots are affected?

Expiry June 30 through July 30, 2026 UPC: 68061710033

Where was it sold?

NY, NJ, PA

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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