Stop using nowFood recall · FDA · Published May 16, 2024
Andersen & Sons Macadamia Nuts Recall: Listeria Contamination Risk
Recalled Andersen & Sons Dry Roasted Macadamia Nuts (25 lbs) due to Listeria monocytogenes contamination. Consumers should avoid eating these nuts to prevent potential illness.
“Andersen & Sons Macadamia Nuts Recall: Listeria Contamination Risk.” GovInfoNow, updated August 17, 2026. https://govinfonow.com/recall/9293-andersen-sons-macadamia-nuts-recall-listeria-contamination-risk. Based on FDA recall #F-1389-2024 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1389-2024%22&limit=1).
Andersen & Sons Shelling, Inc. recalled its Macadamia Nuts, Dry Roasted Style 6 in 25-lb bags due to Listeria monocytogenes contamination, the FDA said on May 16, 2024. The voluntary Class I recall affects 2,850 lbs distributed in Idaho.
How to tell if you have it
Brand: Andersen & Sons
Product: Macadamia Nuts, Dry Roasted Style 6
Size: 25 lbs
Lot code: 26950-1-2-1
Expiration date: 4/12/2025
Distribution: Idaho
The hazard
The product is subject to recall because of potential Listeria monocytogenes contamination. The FDA classified the recall as Class I, indicating a serious health hazard.
Context
GovInfoNow's records show Andersen & Sons Shelling, Inc. has one other recall on record since Sept. 1, 2021, involving Trader Joe's Mixed Nuts packed as Walnuts due to mispackaging on that date. Other recent recalls of similar products include Prima Vera Nueva Butternut Squash Tamales (Dec. 12, 2025), Clover Hill Dairy Soft Cuajada Crumbs (June 1, 2026), and La Colonia Foods Requeson Bulk Product (June 4, 2026).
How to tell if you have this one
Check for the product name 'Andersen & Sons Shelling, Inc. Macadamia Nuts, Dry Roasted Style 6 25 lbs.' with lot code 26950-1-2-1 and expiration date April 12, 2025.
Brand
Andersen & Sons
Category
Food
Based on the official FDA remedy
What to do — step by step
Stop Using Now
Immediately discard any recalled macadamia nuts to prevent potential illness from Listeria monocytogenes.
Where it went and when
Where it was distributed
Distributed in Idaho.
Listed by the agency
Not listed
FDA distribution: “U.S. distribution: ID No foreign distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Idaho.
Recall timeline
FDA terminated this recall 11 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
Official source: FDA Recall #F-1389-2024 (May 16, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1389-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 17, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.