CLASS I Food recall · Reported 9 Aug 2017 · FDA Enforcement Report
IQF White Rice ES CA, Cardboard Tote, product #4621686100 recalled
General Mills is recalling IQF White Rice ES CA, Cardboard Tote, product #4621686100, distributed in Arkansas. The recall was initiated on 19 Jul 2017 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-3336-2017
- FDA event ID
- 77813
- Recalling firm
- General Mills, Minneapolis, MN
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 19 Jul 2017
- FDA classified
- 2 Aug 2017
- Reported
- 9 Aug 2017
- Type
- Voluntary: Firm initiated
- Customers notified by
- Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
- Reason category
- Other Reasons
- Product category
- Rice
Timeline
| 19 Jul 2017 | Recall initiated by company | |
| 2 Aug 2017 | Classified by FDA | +14 days |
| 9 Aug 2017 | Published in enforcement report | +7 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
General Mills was notified by customer of IQF noodles found in IQF rice. The IQF noodles contain eggs and wheat.
Product as listed by the FDA
IQF White Rice ES CA, Cardboard Tote, product #4621686100.
Where it was distributed
AR
Questions about this recall
Why was it recalled?
General Mills was notified by customer of IQF noodles found in IQF rice. The IQF noodles contain eggs and wheat.
Which lots are affected?
22APR7BV
Where was it sold?
AR
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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