CLASS I Food recall · Reported 8 Jun 2022 · FDA Enforcement Report

Dutch Delight Peanut Butter Cup packaged as 10 piece or tub recalled

Walnut Creek Chocolate Co is recalling Dutch Delight Peanut Butter Cup packaged as 10 piece or tub, distributed in 29 states. The recall was initiated on 23 May 2022 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesProduct Codes: DPBC01, DPBC02 Lot Codes: 1334, 2007, 2115, 2007, 2115
Quantity recalled192 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-1150-2022
FDA event ID
90285
Recalling firm
Walnut Creek Chocolate Co, Walnut Creek, OH
Classification
Class I
Status
Terminated
Recall initiated
23 May 2022
FDA classified
2 Jun 2022
Reported
8 Jun 2022
Type
Voluntary: Firm initiated
Customers notified by
E-Mail
Reason category
Salmonella
Product category
Peanut Butter

Timeline

23 May 2022Recall initiated by company
2 Jun 2022Classified by FDA+10 days
8 Jun 2022Published 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

Potential Salmonella contamination

Salmonella causes fever, diarrhea and abdominal cramps, usually 12 to 72 hours after eating contaminated food. Most people recover without treatment, but severe cases can need hospital care.

Product as listed by the FDA

Dutch Delight Peanut Butter Cup packaged as 10 piece or 10oz tub

Where it was distributed

AL, AZ, CA, CO, CT, FL, GA, IA, IL, IN, LA, MA, MI, MN, MO, NC, ND, NM, NV, NY, OH, OK, PA, SC, TN, TX, VA, WI, WV

AlabamaArizonaCaliforniaColoradoConnecticutFloridaGeorgiaIowaIllinoisIndianaLouisianaMassachusettsMichiganMinnesotaMissouriNorth CarolinaNorth DakotaNew MexicoNevadaNew York

Questions about this recall

Is Dutch Delight Peanut Butter Cup packaged as 10 piece or tub recalled?

Yes. Walnut Creek Chocolate Co recalled Dutch Delight Peanut Butter Cup packaged as 10 piece or tub on 23 May 2022. The recall is Class I and its status is Terminated. Recall number F-1150-2022.

Why was it recalled?

Potential Salmonella contamination

Which lots are affected?

Product Codes: DPBC01, DPBC02 Lot Codes: 1334, 2007, 2115, 2007, 2115

Where was it sold?

AL, AZ, CA, CO, CT, FL, GA, IA, IL, IN, LA, MA, MI, MN, MO, NC, ND, NM, NV, NY, OH, OK, PA, SC, TN, TX, VA, WI, WV

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 21 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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