CLASS II Food recall · Reported 17 Apr 2013 · FDA Enforcement Report
Umami Almonds recalled by NatureBox
NatureBox is recalling Umami Almonds. The recall was initiated on 27 Mar 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-1295-2013
- FDA event ID
- 64750
- Recalling firm
- NatureBox, San Carlos, CA
- Brand
- Umami Almonds
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- 27 Mar 2013
- FDA classified
- 5 Apr 2013
- Reported
- 17 Apr 2013
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Undeclared Wheat & Gluten
- Product category
- Milk
Timeline
| 27 Mar 2013 | Recall initiated by company | |
| 5 Apr 2013 | Classified by FDA | +9 days |
| 17 Apr 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
Product may contain wheat allergen. Wheat is not listed in the ingredient statement.
Product as listed by the FDA
NatureBox brand Umami Almonds packed in branded stand-up pouches (whole tamari flavored almonds), Net wt. 4.3 oz. No UPC Codes on the product, Product is processed and packaged by NatureBox, San Carlos, CA; NOTE: Product label DOES declare that it is "Packed in a facility that also processes tree nuts, peanuts, milk, wheat, and soy" below the ingredient statement.
Where it was distributed
Internet sales only.
Questions about this recall
Why was it recalled?
Product may contain wheat allergen. Wheat is not listed in the ingredient statement.
Which lots are affected?
All lot codes with Best By Dates or 5/15/13 or earlier.
Where was it sold?
Internet sales only.
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 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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