CLASS III Food recall · Reported 6 Dec 2023 · FDA Enforcement Report

Chocolate Whoopie Pies recalled by Bisousweet Confections

Bisousweet Confections is recalling Chocolate Whoopie Pies, distributed in Massachusetts, New Hampshire, Oregon. The recall was initiated on 31 Oct 2023 and the FDA has classified it as Class III.

Check your package

Lot, batch or date codesUPC: 851040006329 SKU: 8-CHOC-CLN-CS Manufactured on 10/20/2023 and 10/21/2023
Quantity recalled124 cases containing 4 units each

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-0481-2024
FDA event ID
93352
Recalling firm
Bisousweet Confections, Shirley, MA
Classification
Class III
Status
Terminated
Recall initiated
31 Oct 2023
FDA classified
29 Nov 2023
Reported
6 Dec 2023
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Packaging Defects
Product category
Cakes & Pastries

Timeline

31 Oct 2023Recall initiated by company
29 Nov 2023Classified by FDA+29 days
6 Dec 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

Chocolate Whoopie pie packages contain Raspberry Whoopie pies

Packaging recalls include wrong labels, wrong products in the wrong bottle, missing leaflets, short-filled or empty capsules and seals that fail.

Product as listed by the FDA

Bisousweet Confections Chocolate Whoopie Pies

Where it was distributed

MA, NH, OR

MassachusettsNew HampshireOregon

Questions about this recall

Why was it recalled?

Chocolate Whoopie pie packages contain Raspberry Whoopie pies

Which lots are affected?

UPC: 851040006329 SKU: 8-CHOC-CLN-CS Manufactured on 10/20/2023 and 10/21/2023

Where was it sold?

MA, NH, OR

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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