RecallRadar
FDA · FoodClass I

EAK Distribution LLC food recall: Heirloom Homegrown Green Sprouting Calabrese Broccoli Sprouts Seed.…

Salmonella

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Ongoing
Event ID
100040
Recall initiated
Oct 1, 2026
Classified by FDA
Oct 22, 2026
Posted in Enforcement Report
Oct 28, 2026
Recalling firm
EAK Distribution LLC
Firm location
Casper, WY, United States
Initiated by
Voluntary: Firm initiated
Firm notified customers by
E-Mail
Products in this event
1

What to do

Compare the product name, size, UPC, lot codes and dates below with the product you have. If it matches, do not eat it. Follow the firm's instructions to return it or throw it away.

View the official FDA record ↗

Reason for recall

Salmonella.

What the classification means

  • Class I: FDA's most serious category: there is a reasonable probability that using or being exposed to the product will cause serious health problems or death.

About this recall

The firm started this recall on Oct 1, 2026. FDA classified it 21 days later, on Oct 22, 2026. Distribution reported by FDA: sold on Amazon nationwide

Recalled products (1)

  • H-0174-2027 Class I Ongoing

    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

    Codes / lots: Lot: AUG172026

    Quantity: 3,600 packets (8oz per packet)

Source and freshness

Source
U.S. Food and Drug Administration (FDA) Enforcement Report, via the openFDA food enforcement dataset
Official notice
FDA Enforcement Report, event 100040
Raw record
openFDA API (JSON)
Dataset last updated by FDA
Nov 3, 2026
Imported by RecallRadar
Nov 4, 2026

Enforcement Report entries describe recalls FDA has classified. They are not always the same as a company press release. If something here differs from FDA's record, FDA's record is correct — please tell us.