Del Dee Foods Organic Pea Protein Recall: Salmonella Risk
Del Dee Foods recalls Organic Pea Protein 80% (Lot PP33116-0-D) due to salmonella contamination found in samples before consumer delivery.
Lower-risk recall
Del Dee Foods, Inc.withdrew Lot# PP33116-0-D after receiving a report of salmonella found in two sample tests taken from product in the above lot before it reached the consumer.
Contact the company
What happened, in plain English
Del Dee Foods is recalling Organic Pea Protein 80% (44.1 lbs per paper bag) because salmonella was detected in samples from the specific lot before reaching consumers. This poses a food safety risk if the product is consumed. Read more at govinfonow.com/recall/22465-del-dee-foods-organic-pea-protein-recall-salmonella-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/22465-del-dee-foods-organic-pea-protein-recall-salmonella-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-1383-2017
Cite this page
“Del Dee Foods Organic Pea Protein Recall: Salmonella Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/22465-del-dee-foods-organic-pea-protein-recall-salmonella-risk. Based on FDA recall #F-1383-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1383-2017%22&limit=1).
Why it’s dangerous
Salmonella bacteria can cause food poisoning, leading to symptoms like diarrhea, fever, and abdominal cramps. The contamination was detected in samples before the product reached consumers, indicating a potential food safety hazard.
Who’s affected
Anyone who purchased the recalled lot (PP33116-0-D) of Hemp & Grain Co. Organic Pea Protein 80% from Del Dee Foods. Consumers at highest risk would be those who have eaten the product.
How to tell if you have this one
Check for the lot number PP33116-0-D on the packaging of Hemp & Grain Co. Organic Pea Protein 80% (44.1 lbs per paper bag). The product was sold in paper bags, 36 per pallet.
- Brand
Del Dee Foods- Category
Food
What to do — step by step
Check Product Lot Number
Look for the lot number PP33116-0-D on the packaging to confirm if the product is recalled.
Where it went and when
Where it was distributed
Distributed in 4 states, and outside the U.S.
FDA distribution: “US; MN, CA, NJ, WI. OUS: CANADA” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: California, Minnesota, New Jersey, Wisconsin.
Recall timeline
FDA terminated this recall 2.5 years after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- 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-1383-2017 (January 3, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1383-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 8, 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.