RecallHawk
Class I Recall

Whole Foods Market - Vegan Croissant 4 Count CONTAINS WHEAT, SOY May contain other allergens due to shared production ar

Whole Foods Market Brand 365, Llc

Summary

The FDA issued a Class I for Whole Foods Market - Vegan Croissant 4 Count CONTAINS WHEAT, SOY May contain oth by Whole Foods Market Brand 365, Llc. Reason: Undeclared milk and egg.

Details

Source

Food Recall

External ID

F-0985-2021

Action Date

2021-09-22

Status

Terminated

Category

food

Product Description

Whole Foods Market - Vegan Croissant 4 Count CONTAINS WHEAT, SOY May contain other allergens due to shared production areas, NET WT 0lb 11oz (312g) PLU 69435 packaged in clear plastic container

Lot/Code Info: Packed on 9/2/21; Best by 9/5/2021

Quantity Affected: 8 units

Reason for Recall

Undeclared milk and egg

Distribution

Georgia

Type: Voluntary: Firm initiated

Recall Initiated: 2021-09-03

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 30 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Whole Foods Market Brand 365, Llc has 7 FDA actions in our database, including 7 recalls.

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 (Whole Foods Market Brand 365, Llc) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Whole Foods Market Brand 365, Llc have FDA actions?

Whole Foods Market Brand 365, Llc has 7 FDA actions in our database, including 7 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0985-2021" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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