CLASS I Food recall · Reported 12 Jun 2024 · FDA Enforcement Report

Germantown Dari Whip II, Stabilizer and Emulsifier System recalled

Danisco USA is recalling Germantown Dari Whip II, Stabilizer and Emulsifier System, distributed in 24 states. The recall was initiated on 3 May 2024 and the FDA has classified it as Class I.

Check your package

Lot, batch or date codesLot numbers: 1204602251; 1204602252
Quantity recalled1814.40 kg

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-1310-2024
FDA event ID
94565
Recalling firm
Danisco USA, New Century, KS
Classification
Class I
Status
Terminated
Recall initiated
3 May 2024
FDA classified
6 Jun 2024
Reported
12 Jun 2024
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Salmonella
Product category
Other

Timeline

3 May 2024Recall initiated by company
6 Jun 2024Classified by FDA+34 days
12 Jun 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

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

Germantown Dari Whip II, Stabilizer and Emulsifier System, 22.68 kg / 50 lb bag

Where it was distributed

US: AZ, CA, CO, FL, IA, ID, IL, IN, KS, KY, MI, MN, MO, NE, NJ, NY, OH, OK, PA, TN, TX, UT, VA, WI; Canada, and Mexico

ArizonaCaliforniaColoradoFloridaIowaIdahoIllinoisIndianaKansasKentuckyMichiganMinnesotaMissouriNebraskaNew JerseyNew YorkOhioOklahomaPennsylvaniaTennessee

Questions about this recall

Is Germantown Dari Whip II, Stabilizer and Emulsifier System recalled?

Yes. Danisco USA recalled Germantown Dari Whip II, Stabilizer and Emulsifier System on 3 May 2024. The recall is Class I and its status is Terminated. Recall number F-1310-2024.

Why was it recalled?

Potential Salmonella Contamination

Which lots are affected?

Lot numbers: 1204602251; 1204602252

Where was it sold?

US: AZ, CA, CO, FL, IA, ID, IL, IN, KS, KY, MI, MN, MO, NE, NJ, NY, OH, OK, PA, TN, TX, UT, VA, WI; Canada, and Mexico

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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