Organic Veda Ginger Powder Recall: Salmonella Contamination Risk
Lords Organics recalls Organic Veda ginger powder (24 jars, 16 oz) due to potential Salmonella contamination. Consumers should avoid using affected products.
Lower-risk recall
Lord Organics is recalling ginger powder because it has the potential to be contaminated with Salmonella.
Contact the company
What happened, in plain English
Lords Organics is recalling Organic Veda ginger powder because it may be contaminated with Salmonella. This poses a risk of foodborne illness if consumed. Read more at govinfonow.com/recall/21806-organic-veda-ginger-powder-recall-salmonella-contamination-risk.
Source Summary by GovInfoNow · govinfonow.com/recall/21806-organic-veda-ginger-powder-recall-salmonella-contamination-risk · Updated October 8, 2026 · FDA enforcement record: FDA #F-2236-2017
Cite this page
“Organic Veda Ginger Powder Recall: Salmonella Contamination Risk.” GovInfoNow, updated October 8, 2026. https://govinfonow.com/recall/21806-organic-veda-ginger-powder-recall-salmonella-contamination-risk. Based on FDA recall #F-2236-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-2236-2017%22&limit=1).
Why it’s dangerous
Salmonella is a bacteria that can cause food poisoning. If the ginger powder is contaminated, eating it could lead to symptoms like diarrhea, fever, and stomach cramps.
Who’s affected
Anyone who owns or uses the recalled Organic Veda ginger powder (24 jars, 16 oz) is affected. People with weakened immune systems are at higher risk of foodborne illness.
How to tell if you have this one
Check for the product name 'Organic Veda Ginger Powder', 24 jars, 16 oz (454 grams). The batch number is A324DGRP and the manufacturing date is August 2015.
- Brand
Lords Organics- Category
Food
What to do — step by step
Check Product Details
Look for the batch number A324DGRP and manufacturing date August 2015 on the product label.
Where it went and when
Where it was distributed
Distributed nationwide.
FDA distribution: “US: Nationwide” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA terminated this recall 4 months 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-2236-2017 (April 27, 2017) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-2236-2017 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.