“ZestiGreens Broccoli Seed Recall: Salmonella Risk.” GovInfoNow, updated November 11, 2026. https://govinfonow.com/recall/2075608-fortuna-marketing-inc-recalls-zestigreens-broccoli-seeds-for-sprouting-microgreens. Based on FDA recall #H-0176-2027.
The FDA announced on Sept. 29, 2026, that Fortuna Marketing, Inc. is recalling ZestiGreens Broccoli Seeds for Sprouting due to potential Salmonella contamination. The voluntary Class I recall affects approximately 600 pounds of product distributed primarily to Amazon fulfillment centers.
How to tell if you have it
Brand: ZestiGreens
Product: Broccoli Seeds for Sprouting & Microgreens; Heirloom Broccoli Seeds
SKU: X004IOM4AJ (8 OZ)
SKU: B0D5289F94 (16 OZ)
No lot code
The hazard
The broccoli seeds are potentially contaminated with Salmonella, according to the FDA. The agency classified this as a Class I recall, indicating a high risk of adverse health consequences.
Context
GovInfoNow's records show other recent recalls of similar products include Heirloom Homegrown Broccoli Sprout Seeds Due to Salmonella Risk (2026-10-01), Wild West Seeds Broccoli Recall: Salmonella Risk (2026-09-25), and Gardners Basics Waltham 29 Broccoli Seeds Recalled for Salmonella (2026-09-30).
How to tell if you have this one
Look for ZestiGreens Heirloom Broccoli Seeds in 8-ounce or 16-ounce packages. The specific SKUs are X004IOM4AJ (8 oz) and B0D5289F94 (16 oz). There is no lot code to check.
Brand
ZestiGreens
Category
Food
Based on the official FDA remedy
What to do — step by step
Stop using the seeds
Do not consume or sprout the recalled broccoli seeds due to the potential Salmonella contamination.
Check your purchase history
Verify if you purchased ZestiGreens Broccoli Seeds with SKUs X004IOM4AJ or B0D5289F94, primarily from Amazon.
Contact the manufacturer
The recalling firm notified customers directly; follow any instructions provided by Fortuna Marketing, Inc.
How this recall unfolded
Recall timeline
FDA published this recall 36 days after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4Added to GovInfoNow
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 #H-0176-2027 (September 29, 2026)
Plain-language summary written by qwen3.6:35b-a3b on November 11, 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.