CLASS I Food recall · Reported 26 May 2021 · FDA Enforcement Report
Caramel Rice Cakes 14 rice cakes per packaging Brands recalled
Basic Grain Products is recalling Caramel Rice Cakes 14 rice cakes per packaging Brands: Kroger Brand and Stop & Shop, distributed in Colorado, Connecticut, Kansas, Pennsylvania. The recall was initiated on 21 Apr 2021 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-0545-2021
- FDA event ID
- 87801
- Recalling firm
- Basic Grain Products, Coldwater, OH
- Brand
- Kroger
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 21 Apr 2021
- FDA classified
- 20 May 2021
- Reported
- 26 May 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Undeclared Milk
- Product category
- Crackers
Timeline
| 21 Apr 2021 | Recall initiated by company | |
| 20 May 2021 | Classified by FDA | +29 days |
| 26 May 2021 | 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
Undeclared Milk Allergen
Product as listed by the FDA
Caramel Rice Cakes 6.56oz (186g) 12 units per case 14 rice cakes per packaging Brands: Kroger Brand and Stop & Shop Brand
Where it was distributed
Kroger distribution centers in KS, CO, IN Stop & Shop distribution centers in PA, CT
Questions about this recall
Why was it recalled?
Undeclared Milk Allergen
Which lots are affected?
Lot Codes: DEC1521, DEC1621 UPC: 011110357922, 688267076152
Where was it sold?
Kroger distribution centers in KS, CO, IN Stop & Shop distribution centers in PA, CT
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 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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