CLASS II Food recall · Reported 12 Dec 2018 · FDA Enforcement Report

Chocolate and Nut Tray recalled by First Source

First Source is recalling Chocolate and Nut Tray, distributed in Massachusetts, Maryland, New Jersey, New York, Pennsylvania, Virginia. The recall was initiated on 20 Nov 2018 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesBest Before 7/9/19
Quantity recalled229 cases

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-0691-2019
FDA event ID
81611
Recalling firm
First Source, Tonawanda, NY
Classification
Class II
Status
Terminated
Recall initiated
20 Nov 2018
FDA classified
4 Dec 2018
Reported
12 Dec 2018
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Tree Nuts
Product category
Chocolate

Timeline

20 Nov 2018Recall initiated by company
4 Dec 2018Classified by FDA+14 days
12 Dec 2018Published 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 contains undeclared pecans and cashews.

Product as listed by the FDA

Chocolate and Nut Tray. The product comes in a four-quadrant plastic tray, NET WT 37 OZ (2 LBS 5 OZ) 1.05KG, with UPC: 0 23637 43369 0.

Where it was distributed

MA, MD, NJ, NY, PA, VA

MassachusettsMarylandNew JerseyNew YorkPennsylvaniaVirginia

Questions about this recall

Why was it recalled?

Product contains undeclared pecans and cashews.

Which lots are affected?

Best Before 7/9/19

Where was it sold?

MA, MD, NJ, NY, PA, VA

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 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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