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
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
- Brand
- Germantown Dari
- 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 2024 | Recall initiated by company | |
| 6 Jun 2024 | Classified by FDA | +34 days |
| 12 Jun 2024 | Published 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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