CLASS II Food recall · Reported 4 Aug 2021 · FDA Enforcement Report
Del Monte Fresh Cut Golden Sweet Whole Kernel Corn recalled
Del Monte Foods is recalling Del Monte Fresh Cut Golden Sweet Whole Kernel Corn, distributed in 19 states. The recall was initiated on 22 Jun 2021 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-0808-2021
- FDA event ID
- 88228
- Recalling firm
- Del Monte Foods, Walnut Creek, CA
- Brand
- Del Monte
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 22 Jun 2021
- FDA classified
- 29 Jul 2021
- Reported
- 4 Aug 2021
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Mold
- Product category
- Nuts
Timeline
| 22 Jun 2021 | Recall initiated by company | |
| 29 Jul 2021 | Classified by FDA | +37 days |
| 4 Aug 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
Firm discovered that some containers exhibited post-process spoilage during additional inspection and deployment of product at Distribution Center.
Product as listed by the FDA
Del Monte Fresh Cut Golden Sweet Whole Kernel Corn; 15.25 oz. can (24 x 15.25 oz. cans per case) Case UPC 10024000163029 Can UPC - 024000163022 Distributed by Del Monte Foods, Walnut Creek, CA
Where it was distributed
AL, AR, IA, IL, IN, KS, KY, LA, MI, MN, MO, MS, ND, NE, OH, PA, TN, WI, WV
AlabamaArkansasIowaIllinoisIndianaKansasKentuckyLouisianaMichiganMinnesotaMissouriMississippiNorth DakotaNebraskaOhioPennsylvaniaTennesseeWisconsinWest Virginia
Questions about this recall
Is Del Monte Fresh Cut Golden Sweet Whole Kernel Corn recalled?
Yes. Del Monte Foods recalled Del Monte Fresh Cut Golden Sweet Whole Kernel Corn on 22 Jun 2021. The recall is Class II and its status is Terminated. Recall number F-0808-2021.
Why was it recalled?
Firm discovered that some containers exhibited post-process spoilage during additional inspection and deployment of product at Distribution Center.
Which lots are affected?
Lot Number Best If Used By 1064BD 01 MAR 2024 1067BD 01 MAR 2024 1068BD 01 MAR 2024 1069BD 01 MAR 2024 1070BD 01 MAR 2024
Where was it sold?
AL, AR, IA, IL, IN, KS, KY, LA, MI, MN, MO, MS, ND, NE, OH, PA, TN, WI, WV
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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