CLASS II Food recall · Reported 10 Jul 2013 · FDA Enforcement Report
Dixie Lily Stone Ground Meal recalled by Hoover Mill
Hoover Mill is recalling Dixie Lily Stone Ground Meal, distributed in Alabama. The recall was initiated on 10 Apr 2013 and the FDA has classified it as Class II.
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-1580-2013
- FDA event ID
- 65446
- Recalling firm
- Hoover Mill, Chipley, FL
- Brand
- Dixie Lily
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 10 Apr 2013
- FDA classified
- 28 Jun 2013
- Reported
- 10 Jul 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Other Reasons
- Product category
- Other
Timeline
| 10 Apr 2013 | Recall initiated by company | |
| 28 Jun 2013 | Classified by FDA | +79 days |
| 10 Jul 2013 | Published in enforcement report | +12 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Due to high levels of aflatoxin
Product as listed by the FDA
Dixie Lily Stone Ground Meal 24 oz & 5lbs
Where it was distributed
Alabama
Questions about this recall
Is Dixie Lily Stone Ground Meal recalled?
Yes. Hoover Mill recalled Dixie Lily Stone Ground Meal on 10 Apr 2013. The recall is Class II and its status is Terminated. Recall number F-1580-2013.
Why was it recalled?
Due to high levels of aflatoxin
Which lots are affected?
24 oz-UPC #05663-10739 Lot # "Sell By 2-27-14" ; 5 lbs.-UPC #05663-10239 Lot # "Sell By 3-1-14"
Where was it sold?
Alabama
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 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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