CLASS II Food recall · Reported 8 Nov 2017 · FDA Enforcement Report

Wegmans Marshmellow Treat recalled by Wegmans Food Markets

Wegmans Food Markets is recalling Wegmans Marshmellow Treat, distributed in Massachusetts, Maryland, New Jersey, New York, Pennsylvania, Virginia. The recall was initiated on 26 Oct 2017 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesSold prior to October 26, 2017
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-0101-2018
FDA event ID
78388
Recalling firm
Wegmans Food Markets, Rochester, NY
Classification
Class II
Status
Terminated
Recall initiated
26 Oct 2017
FDA classified
2 Nov 2017
Reported
8 Nov 2017
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Soy
Product category
Other

Timeline

26 Oct 2017Recall initiated by company
2 Nov 2017Classified by FDA+7 days
8 Nov 2017Published in enforcement report+6 days

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

Reason for recall

Products contain undeclared soy lecithin

Product as listed by the FDA

Wegmans Marshmellow Treat sold by the pound UPC: 2-08012-00000

Where it was distributed

NJ, NY, MD, MA, PA, VA,

MassachusettsMarylandNew JerseyNew YorkPennsylvaniaVirginia

Stores named: Wegmans

Questions about this recall

Is Wegmans Marshmellow Treat recalled?

Yes. Wegmans Food Markets recalled Wegmans Marshmellow Treat on 26 Oct 2017. The recall is Class II and its status is Terminated. Recall number F-0101-2018.

Why was it recalled?

Products contain undeclared soy lecithin

Which lots are affected?

Sold prior to October 26, 2017

Where was it sold?

NJ, NY, MD, MA, 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 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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