Lower riskFood recall · FDA · Published December 31, 2025
WFM Purchasing Brussel Sprouts & Kale Slaw Recall: Undeclared Fish and Egg Allergen Hazard
WFM Purchasing recalls Bruss: Sprouts & Kale Slaw due to undeclared fish and egg allergens. Consumers should check product labels for allergen information.
“WFM Purchasing Brussel Sprouts & Kale Slaw Recall: Undeclared Fish and Egg Allergen Hazard.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/6848-wfm-purchasing-brussel-sprouts-kale-slaw-recall-undeclared-fish-and. Based on FDA recall #H-0403-2026.
WFM Purchasing, LP voluntarily recalled 88 units of Brussel Sprouts & Kale Slaw due to undeclared fish and egg allergens, the FDA said on Dec. 31, 2025. The Class I recall affects products distributed in New York, New Jersey, and Virginia.
How to tell if you have it
Brand: WFM Purchasing
Product: Brussel Sprouts & Kale Slaw
Quantity: 88 units
Distribution: New York, New Jersey, Virginia
The hazard
The product contains undeclared fish and egg allergens. The FDA classified this as a Class I recall, indicating a reasonable probability that the food will cause serious adverse health consequences or death.
Context
GovInfoNow's records show WFM Purchasing, LP has four other recalls on file since Sept. 9, 2025. Other recent recalls of similar products include Koi Koi Trading Fish Balls Recall (Jan. 28, 2026), Gellert Global Group Kimbap Recall (June 25, 2026), and Pearl Milling Pancake Mix Recall (May 13, 2026).
How to tell if you have this one
The recalled product is Brussel sprouts and kale slaw with no specific code or model number listed. Check for the brand name WFM Purchasing on the packaging.
Brand
WFM Purchasing
Category
Food
Based on the official FDA remedy
What to do — step by step
Check Product Label
Look for the brand name WFM Purchasing on the packaging to identify if the product is recalled.
Where it went and when
Where it was distributed
Distributed in 3 states.
Listed by the agency
Not listed
FDA distribution: “New York, New Jersey and Virginia” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: New Jersey, New York, Virginia.
Recall timeline
FDA terminated this recall 9 months after the firm started it.
1Firm started the recall
2FDA classified it Class I
3Published in FDA’s Enforcement Report
4FDA terminated the recall
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-0403-2026 (December 31, 2025)
Plain-language summary written by qwen3:4b on August 18, 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.