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FDA · FoodClass I

Berlin Seeds food recall: Berlin Seeds Alfalfa Sprouting Seeds

SalmonellaE. coliMicrobial contamination

Key facts

Agency
U.S. Food and Drug Administration (FDA)
Program
Food
Classification
Class I
Status
Ongoing
Event ID
99894
Recall initiated
Sep 12, 2026
Classified by FDA
Oct 6, 2026
Posted in Enforcement Report
Oct 14, 2026
Recalling firm
Berlin Seeds
Firm location
Millersburg, OH, 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

Product contains alfalfa seed recalled by the supplier due to potential E. coli and/or Salmonella contamination.

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 Sep 12, 2026. FDA classified it 24 days later, on Oct 6, 2026. Distribution reported by FDA: Through the firm's retail store in Millersburg, OH and nationwide through the firm's website

Recalled products (1)

  • H-0013-2027 Class I Ongoing

    Berlin Seeds Alfalfa Sprouting Seeds, packaged in 1/4 lb., 1/2 lb., 1 lb., and 5 lb. resealable bags and 50 lb. woven poly bags

    Codes / lots: Lot # SAL2-24JB (on 5 lb. and 50 lb. bags only)

    Quantity: 950 lbs.

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 99894
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.