RecallHawk
Class I Recall

WHOLE FOODS MARKET red lentil dal NET WT. 12 OZ (340g) DISTRIBUTED BY: WHOLE FOODS MARKET AUSTIN, TX 78703 UPC 1 95515 0

Bakkavor Foods USA Inc.

Summary

The FDA issued a Class I for WHOLE FOODS MARKET red lentil dal NET WT. 12 OZ (340g) DISTRIBUTED BY: WHOLE FOO by Bakkavor Foods USA Inc.. Reason: Possible Listeria monocytogenes in product.

Details

Source

Food Recall

External ID

F-1043-2022

Action Date

2022-05-11

Status

Terminated

Category

food

Product Description

WHOLE FOODS MARKET red lentil dal NET WT. 12 OZ (340g) DISTRIBUTED BY: WHOLE FOODS MARKET AUSTIN, TX 78703 UPC 1 95515 02394 8

Lot/Code Info: USE BY 4/15/2022, USE BY 4/17/2022, USE BY 4/18/2022, USE BY 4/19/2022, USE BY 4/22/2022, USE BY 4/24/2022, USE BY 4/25/2022 & USE BY 4/26/2022

Quantity Affected: 3,855 cs/4/12 oz trays

Reason for Recall

Possible Listeria monocytogenes in product

Distribution

Product was shipped to the following states: CA, CO, CT. FL, GA, IL, MD, TX & WA.

Type: Voluntary: Firm initiated

Recall Initiated: 2022-04-19

Company

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

Bakkavor Foods USA Inc. has 3 FDA actions in our database, including 3 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 (Bakkavor Foods USA Inc.) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Bakkavor Foods USA Inc. have FDA actions?

Bakkavor Foods USA Inc. has 3 FDA actions in our database, including 3 recalls and 0 device clearances.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-1043-2022" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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