Wild West Seeds Broccoli Seeds Green Sprouting Calabrese lot #4105. Net Wt. 50lb. Wild West Seeds Broccoli Waltham29 See
Summary
The FDA issued a Class I for Wild West Seeds Broccoli Seeds Green Sprouting Calabrese lot #4105. Net Wt. 50lb by Wild West Seed Inc. Reason: Salmonella.
Details
Source
Food Recall
External ID
H-0171-2027
Action Date
2026-10-28
Status
Ongoing
Category
food
Product Description
Wild West Seeds Broccoli Seeds Green Sprouting Calabrese lot #4105. Net Wt. 50lb. Wild West Seeds Broccoli Waltham29 Seeds lot #4475 (this lot was sent to only one consignee). Net Wt. 50lb.
Lot/Code Info: Lot #W4105. Lot #W4475 (same as lot #W4105 but it changed due to one consignee's request).
Quantity Affected: 9,476 lbs.
Reason for Recall
Salmonella
Distribution
Distributed in CA, FL, GA, ID, MD, ME, NC, OR, PA, TX, UT, and United Kingdom.
Type: Voluntary: Firm initiated
Recall Initiated: 2026-09-25
Company
Albany, OR
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 (Wild West Seed Inc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.
How often does Wild West Seed Inc have FDA actions?
This is the only FDA action we have on record for Wild West Seed Inc in our database.
Where can I find the official FDA record?
The official record is available on FDA.gov. Search for "H-0171-2027" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.
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