CLASS I Food recall · Reported 10 Jul 2013 · FDA Enforcement Report

Hanna ford Gourmet Cookie Platter package) recalled

Delhaize America (Hannaford Bros) is recalling Hanna ford Gourmet Cookie Platter package), Includes oatmeal raisin cookies, distributed in Massachusetts, Maine, New Hampshire, New York, Vermont. The recall was initiated on 4 May 2013 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesSold at retail bakery through 5/6/13
Quantity recalled154 platters (36 oz)

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-1588-2013
FDA event ID
65151
Recalling firm
Delhaize America (Hannaford Bros), South Portland, ME
Brand
Hanna
Classification
Class I
Status
Terminated
Recall initiated
4 May 2013
FDA classified
2 Jul 2013
Reported
10 Jul 2013
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Undeclared Tree Nuts
Product category
Cookies

Timeline

4 May 2013Recall initiated by company
2 Jul 2013Classified by FDA+59 days
10 Jul 2013Published 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

Cookies may contain undeclared tree nuts

Product as listed by the FDA

Hanna ford Gourmet Cookie Platter (36 oz. package), Includes oatmeal raisin cookies UPC # 04126874662

Where it was distributed

Maine, New Hampshire, Vermont, New York and Massachusetts.

MassachusettsMaineNew HampshireNew YorkVermont

Stores named: Food Lion

Questions about this recall

Why was it recalled?

Cookies may contain undeclared tree nuts

Which lots are affected?

Sold at retail bakery through 5/6/13

Where was it sold?

Maine, New Hampshire, Vermont, New York and Massachusetts.

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 I mean?

Class I is the most serious FDA recall category: there is a reasonable probability that using the product will cause serious health consequences or death.

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.

Other products in this recall event

1 other product · FDA event 65151

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