CLASS III Food recall · Reported 15 Feb 2023 · FDA Enforcement Report

Back To Nature Plant Based Snacks Fudge Mint Cookies recalled

B&G Foods North America is recalling Back To Nature Plant Based Snacks Fudge Mint Cookies, distributed in Florida, Illinois, Indiana. The recall was initiated on 19 Jan 2023 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesOCT022023 OCT032023 OCT042023
Quantity recalled115 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-0343-2023
FDA event ID
91536
Recalling firm
B&G Foods North America, Parsippany, NJ
Brand
Back To
Classification
Class III
Status
Terminated
Recall initiated
19 Jan 2023
FDA classified
8 Feb 2023
Reported
15 Feb 2023
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Undeclared Peanuts
Product category
Cookies

Timeline

19 Jan 2023Recall initiated by company
8 Feb 2023Classified by FDA+20 days
15 Feb 2023Published in enforcement report+7 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 peanut residue.

Product as listed by the FDA

Back To Nature Plant Based Snacks Fudge Mint Cookies Net Wt. 6.4 OZ. (181g) UPC code: 819898011025

Where it was distributed

Distributed to distributors in IL, IN, and FL.

FloridaIllinoisIndiana

Questions about this recall

Why was it recalled?

Cookies may contain undeclared peanut residue.

Which lots are affected?

OCT022023 OCT032023 OCT042023

Where was it sold?

Distributed to distributors in IL, IN, and FL.

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 III mean?

Class III recalls are for products unlikely to cause any adverse health consequence, usually labelling or quality issues.

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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