Kerry Soy Honey Cluster 30lb Case Recall: Salmonella Risk from Shared Equipment
Kerry Inc recalls Soy Honey Cluster 30lb cases due to potential salmonella contamination from shared equipment with a previous outbreak. Affected lots expire by 10/30/18 to 11/2/18.
Lower-risk recall
an ingredient in this product was manufactured during the time-frame and on the same piece of equipment that was associated with a salmonella outbreak.
Contact the company
What happened, in plain English
Kerry Inc is recalling Soy Honey Cluster 30-pound cases because they were made on equipment that caused a salmonella outbreak. This could lead to food poisoning if the product is consumed. Read more at govinfonow.com/recall/18998-kerry-soy-honey-cluster-30lb-case-recall-salmonella-risk-from.
Source Summary by GovInfoNow · govinfonow.com/recall/18998-kerry-soy-honey-cluster-30lb-case-recall-salmonella-risk-from · Updated October 6, 2026 · FDA enforcement record: FDA #F-1787-2018
Cite this page
“Kerry Soy Honey Cluster 30lb Case Recall: Salmonella Risk from Shared Equipment.” GovInfoNow, updated October 6, 2026. https://govinfonow.com/recall/18998-kerry-soy-honey-cluster-30lb-case-recall-salmonella-risk-from. Based on FDA recall #F-1787-2018 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1787-2018%22&limit=1).
Why it’s dangerous
The product was manufactured on equipment that previously caused a salmonella outbreak. This means the same equipment could have contaminated the product with harmful bacteria.
Who’s affected
People who bought Kerry's Soy Honey Cluster 30lb cases with lot numbers 0503825701 through 0506825701 (expiring 10/30/18 to 11/2/18) are affected. Those who have consumed the product may face food poisoning risks.
How to tell if you have this one
Check for the product code 30666529.137 on the box. Look for lot numbers 0503825701 to 0506825701 with expiration dates from 10/30/18 to 11/2/18.
- Brand
Kerry- Category
Food
What to do — step by step
Check Product Details
Look for the product code 30666529.137 and lot numbers 0503825701 to 0506825701 on the box.
Where it went and when
Where it was distributed
Distributed in Minnesota.
FDA distribution: “MN” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Minnesota.
Recall timeline
FDA terminated this recall 8 months after the firm started it.
- Firm started the recall
- Published in FDA’s Enforcement Report
- FDA classified it Class II
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
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-1787-2018 (July 12, 2018) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1787-2018 to see it in context.
- Plain-language summary written by qwen3:4b on October 6, 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.