CLASS II Food recall · Reported 24 Jan 2024 · FDA Enforcement Report

Neiman Marcus Christmas Petit Fours 24pc recalled by Sweet Shop Candies

Sweet Shop Candies is recalling Neiman Marcus Christmas Petit Fours 24pc, distributed in 17 states. The recall was initiated on 8 Dec 2023 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codes33050163
Quantity recalled1488 units

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-0774-2024
FDA event ID
93635
Recalling firm
Sweet Shop Candies, Mount Pleasant, TX
Classification
Class II
Status
Terminated
Recall initiated
8 Dec 2023
FDA classified
18 Jan 2024
Reported
24 Jan 2024
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Mold
Product category
Other

Timeline

8 Dec 2023Recall initiated by company
18 Jan 2024Classified by FDA+41 days
24 Jan 2024Published 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

mold and yeast in product

Product as listed by the FDA

Neiman Marcus Christmas Petit Fours 24pc

Where it was distributed

Product was distributed to one distribution center. Then to retail stores in TX, PA, CA, MO, IL, VA, NC, NJ, FL, CO, GA, NY, NV, MA, MI, HI, AZ

ArizonaCaliforniaColoradoFloridaGeorgiaHawaiiIllinoisMassachusettsMichiganMissouriNorth CarolinaNew JerseyNevadaNew YorkPennsylvaniaTexasVirginia

Questions about this recall

Why was it recalled?

mold and yeast in product

Which lots are affected?

33050163

Where was it sold?

Product was distributed to one distribution center. Then to retail stores in TX, PA, CA, MO, IL, VA, NC, NJ, FL, CO, GA, NY, NV, MA, MI, HI, AZ

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.

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