The Recall Desk
Agency classClass IOur severity:CriticalFDA (Food)·F-0375-2020·Announced 2019-12-25

Whole Foods Recalls Ethiopian Cauliflower Broccoli for Listeria Risk

Whole Foods Market is recalling Ethiopian Cauliflower Broccoli served on the hot bar due to possible Listeria monocytogenes contamination.

The agency’s classification

FDA (Food): Class I

Class I is a situation in which there is a reasonable probability that the use of or exposure to a violative product will cause serious adverse health consequences or death.

This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work

What this means for you

Our assessment, not the agency’s: severity 5/5 (Critical).

Highest-severity recall. The hazard can cause serious injury or death. Stop using the product now and follow the agency's instructions.

Our severity reasoning: The source metadata explicitly identifies this as an FDA Class I recall, which mandates a severity score of 5 according to the rubric.

Plain-English summary

Whole Foods Market is recalling Ethiopian Cauliflower Broccoli served on the hot bar. The recall is due to possible contamination with Listeria monocytogenes.

The affected product was sold on the hot bar from October 10, 2019, through November 4, 2019. The total quantity involved is 12,898 lbs, and the distribution was nationwide.

Consumers who purchased this product should discard it or return it to the store of purchase.

The recalled product

Product
CAULIFLOWER BROCCOLI ETHIOPIAN served on the hot bar
Manufacturer
Whole Foods Market
Hazard

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Sold on the hot bar from Oct.10.2019 through Nov. 4.2019

Distribution

Distributed nationwide across the United States.

Part of a larger recall action

This product is one of 57 recalled by Whole Foods Market under a single FDA (Food) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.

See all 57 products in this recall →

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