CLASS II Food recall · Reported 17 Apr 2019 · FDA Enforcement Report

Peanut Butter Cookies recalled by Thomas Hammer Coffee Roasters

Thomas Hammer Coffee Roasters is recalling Peanut Butter Cookies, distributed in Idaho, Washington. The recall was initiated on 27 Mar 2019 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesCOOK-PEANU
Quantity recalled100 cookies

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-1239-2019
FDA event ID
82515
Recalling firm
Thomas Hammer Coffee Roasters, Spokane, WA
Classification
Class II
Status
Terminated
Recall initiated
27 Mar 2019
FDA classified
5 Apr 2019
Reported
17 Apr 2019
Type
Voluntary: Firm initiated
Customers notified by
Telephone
Reason category
Undeclared Milk
Product category
Cookies

Timeline

27 Mar 2019Recall initiated by company
5 Apr 2019Classified by FDA+9 days
17 Apr 2019Published in enforcement report+12 days

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

Reason for recall

Peanut Butter Cookies is recalled because the Ingredients Statement declared butter but did not declare milk.

Product as listed by the FDA

Peanut Butter Cookies

Where it was distributed

distributed in ID and WA.

IdahoWashington

Questions about this recall

Why was it recalled?

Peanut Butter Cookies is recalled because the Ingredients Statement declared butter but did not declare milk.

Which lots are affected?

COOK-PEANU

Where was it sold?

distributed in ID and WA.

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.

Other products in this recall event

2 other products · FDA event 82515

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