Heirloom Homegrown Green Sprouting Calabrese Broccoli Sprouts Seed. Net wt. 8oz ASIN #B09P49WHHP, UPC 8 50056 62744 3. E
Summary
The FDA issued a Class I for Heirloom Homegrown Green Sprouting Calabrese Broccoli Sprouts Seed. Net wt. 8oz by EAK Distribution LLC. Reason: Salmonella..
Details
Source
Food Recall
External ID
H-0174-2027
Action Date
2026-10-28
Status
Ongoing
Category
food
Product Description
Heirloom Homegrown Green Sprouting Calabrese Broccoli Sprouts Seed. Net wt. 8oz ASIN #B09P49WHHP, UPC 8 50056 62744 3. EAK Distribution LLC 5830 E. 2nd St. PMB 91446 Casper, WY 82609 Label with Growing Instructions ***Easy to Grow ***Up to 24 Servings***90%+ Germination Rates***Shelf Stable for 2+ Years
Lot/Code Info: Lot: AUG172026
Quantity Affected: 3,600 packets (8oz per packet)
Reason for Recall
Salmonella.
Distribution
sold on Amazon nationwide
Type: Voluntary: Firm initiated
Recall Initiated: 2026-10-01
Company
Casper, WY
Context & Analysis
This is a Class I recall. Class I recalls are the most serious — there is a reasonable probability that use of or exposure to the product will cause serious health consequences or death.
This was one of 82 food recalls issued in the same week, part of 117 food-related FDA actions this month.
Frequently Asked Questions
What is a Class I recall?
A Class I recall is the most serious type. The FDA has determined there is a reasonable probability that the product will cause serious adverse health consequences or death. Consumers should stop using the product immediately.
What should I do if I have this product?
Stop using the product. Check the product against the specific lot numbers or identifiers listed in the recall. Contact the manufacturer (EAK Distribution LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does EAK Distribution LLC have FDA actions?
This is the only FDA action we have on record for EAK Distribution LLC in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0174-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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