CLASS I Food recall · Reported 14 Aug 2024 · FDA Enforcement Report
Shelled Walnuts package in plastic flexible packaging recalled
Stutz Packing is recalling Shelled Walnuts package in plastic flexible packaging, distributed in Arizona, Texas. The recall was initiated on 8 Jul 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-1651-2024
- FDA event ID
- 94991
- Recalling firm
- Stutz Packing, Indio, CA
- Brand
- Shelled Walnuts
- Classification
- Class I
- Status
- Terminated
- Recall initiated
- 8 Jul 2024
- FDA classified
- 6 Aug 2024
- Reported
- 14 Aug 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Reason category
- Listeria
- Product category
- Nuts
Timeline
| 8 Jul 2024 | Recall initiated by company | |
| 6 Aug 2024 | Classified by FDA | +29 days |
| 14 Aug 2024 | Published in enforcement report | +8 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Shelled walnuts tested positive for Listeria
Listeria monocytogenes can grow at refrigerator temperatures. Infection is most dangerous for pregnant women, newborns, older adults and people with weakened immune systems. Symptoms can appear up to 70 days after eating contaminated food.
Product as listed by the FDA
Shelled Walnuts 1lb package in plastic flexible packaging. 24 packages per case
Where it was distributed
TX, AZ. No foreign distributors.
Questions about this recall
Why was it recalled?
Shelled walnuts tested positive for Listeria
Which lots are affected?
Lot 24171 1 & Lot 24172 1 UPC 7 15001 00908 1
Where was it sold?
TX, AZ. No foreign distributors.
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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