RecallHawk
Class II Recall

Karma White Cheddar Cheese Popped Water Lily Seeds packed in 1.5oz pouches UPC: 617201892589

Karma Spices and Trading Company, LLC

Summary

The FDA issued a Class II for Karma White Cheddar Cheese Popped Water Lily Seeds packed in 1.5oz pouches UPC: by Karma Spices and Trading Company, LLC. Reason: Undeclared milk.

Details

Source

Food Recall

External ID

F-0769-2023

Action Date

2023-05-03

Status

Terminated

Category

food

Product Description

Karma White Cheddar Cheese Popped Water Lily Seeds packed in 1.5oz pouches UPC: 617201892589

Lot/Code Info: Lot numbers: 051222, 082222, 111622, 021323

Quantity Affected: 1423 units

Reason for Recall

Undeclared milk

Distribution

Michigan and online at www.karmawellnesskitchen.com

Type: Voluntary: Firm initiated

Recall Initiated: 2023-04-05

Context & Analysis

This is a Class II recall. Class II recalls indicate that use of or exposure to the product may cause temporary or medically reversible health consequences, or that the probability of serious consequences is remote.

This was one of 28 food recalls issued in the same week, part of 204 food-related FDA actions this month.

Frequently Asked Questions

What is a Class II recall?

A Class II recall means the product may cause temporary or medically reversible adverse health consequences, or the probability of serious adverse consequences is remote. Consumers should discontinue use.

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 (Karma Spices and Trading Company, LLC) or your retailer for a refund or replacement. If you experienced adverse effects, report them to the FDA via MedWatch.

How often does Karma Spices and Trading Company, LLC have FDA actions?

This is the only FDA action we have on record for Karma Spices and Trading Company, LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "F-0769-2023" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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